WorldWideScience

Sample records for chemical hydrogen cyanamide

  1. Effects of Hydrogen Cyanamide Application Rates and Timing on Fruit and Foliage of 'Climax' Rabbiteye Blueberry

    Science.gov (United States)

    A field study was conducted to evaluate the effects of flower bud pruning or utilizing differing rates of hydrogen cyanamide, on development of vegetative and floral buds, as well as on leaf area, vegetative coverage, fruit damage and development, and yield. In this study, hydrogen cyanamide applica...

  2. CYANAMIDE: A POSSIBLE KEY COMPOUND IN CHEMICAL EVOLUTION

    Energy Technology Data Exchange (ETDEWEB)

    Steinman, Gary; Lemmon, Richard M.; Calvin, Melvin

    1964-05-01

    The prebiotic synthesis of phosphorus-containing compounds--such as nucleotides and polynucleotides--would require both a geologically plausible source of the element and pathways for its incorporation into chemical systems on the primitive Earth. The mineral apatite, which is the only significant source of phosphate on Earth, has long been thought to be problematical in this respect due to its low solubility and reactivity. However, in the last decade or so, at least two pathways have been demonstrated which would circumvent these perceived problems. In addition, recent results would seem to suggest an additional, extraterrestrial source of reactive phosphorus. It appears that the 'phosphorus problem' is no longer the stumbling block which it was once thought to be.

  3. Hydrogen cyanamide on citrus: Phytotoxicity, influences on flush in potted and field trees and effects on bloom and cropload in the field

    Science.gov (United States)

    Bloom in individual citrus trees typically continues for more than a month in south Florida. Prolonged bloom increases susceptibility to postbloom fruit drop disease (caused by Colletotrichum acutatum) and contributes to variable fruit maturity at harvest. Hydrogen cyanamide (HCN) is used to acceler...

  4. Efeito de época de poda, cianamida hidrogenada e irrigação na produção antecipada de figos verdes Effect of pruning time, hydrogenated cyanamide and irrigation upon anticipated production of green figs

    Directory of Open Access Journals (Sweden)

    Paulo Márcio Norberto

    2001-11-01

    Full Text Available O objetivo deste trabalho foi avaliar o efeito de época de poda, aplicação de cianamida hidrogenada (Dormex e de irrigação no desenvolvimento da figueira (Ficus carica L. cultivar Roxo de Valinhos e na produção antecipada de frutos verdes para indústria. Os tratamentos constaram de: dez épocas de poda, com intervalos de 15 dias; aplicação de solução a 2% de cianamida hidrogenada; aplicação de cianamida hidrogenada + irrigação; e irrigação três vezes por semana, fornecendo 40 L de água/planta/dia. As plantas podadas na segunda quinzena de maio, irrigadas, e que receberam cianamida hidrogenada, apresentaram maior número médio de frutos, e maior comprimento dos ramos, e produziram frutos na entressafra (outubro; nas podas mais precoces (primeira quinzena de abril até a segunda quinzena de maio houve um prolongamento no ciclo das plantas, embora a primeira quinzena de abril tenha possibilitado a colheita de figos na entressafra; nas épocas de poda mais tardias (primeira quinzena de junho até a segunda quinzena de agosto, os tratamentos cianamida hidrogenada + irrigação, e somente irrigação, apresentaram maior comprimento de ramo e maior número de frutos, mas as colheitas foram iniciadas no período normal da safra.The objective of this work was to evaluate the effect of the pruning time, the application of hydrogenated cyanamide (Dormex, and of the irrigation on plant development and on the premature production of green figs (Ficus carica L., cultivar Roxo de Valinhos, for the industry. Treatments consisted of ten pruning times, with intervals of 15 days, application of the solution at 2% of hydrogenated cyanamide, application of hydrogenated cyanamide + irrigation, and irrigation three times a week, supplying 40 L of water/plant/day. The pruned plants at the May's second fortnight, which were irrigated and received hydrogenated cyanamide, presented a larger number of fruits as average, larger branch length, and

  5. Estimation of chilling requirement and effect of hydrogen cyanamide on budbreak and fruit characteristics of 'superior seedless' table grape cultivated in a mild winter climate

    International Nuclear Information System (INIS)

    The chilling requirement and optimum time for hydrogen cyanamide (HC) application were determined for Superior Seedless table grape grown in southern Tunisia, an arid mild winter region. The reliability of five models to predict chilling accumulation for this cultivar was also investigated. In mid-November, current season shoots were excised and subjected to artificial chilling at 7 deg. C for different lengths of time. Each time, half the shoots were treated with a 2% (v/v) aqueous solution of HC, the others were sprayed with distilled water. Thereafter, these shoots were forced to budburst. Rest intensity gradually declined due to chilling accumulation. We estimated that the cultivar needed approx. 440 hours (h) of chilling, or chilling requirement (CR), to overcome endodormancy. During two dormant seasons, estimation of chilling accumulation showed that the Positive Chill Unit model was the most suitable to predict rest completion for Superior Seedless grown under our climatic conditions. Using this model, we found that the variety's CR was not always met by mid-February. In both laboratory and field trials, HC was most effective in enhancing and advancing budbreak if applied when approx. 2/3 of the cultivar's CR were met. Moreover, by this application berry weight and diameter were increased and fruit maturity was advanced. Our study indicated that HC (2%) was effective in advancing budbreak and fruit maturity of Superior Seedless table grape although its effectiveness depended on application date. (author)

  6. Enraizamento de estacas apicais lenhosas de figueira 'Roxo de Valinhos'com aplicação de AIB e cianamida hidrogenada Rooting of apical hardwood cuttings of fig tree 'Roxo de Valinhos' with application of IBA and hydrogen cyanamide

    Directory of Open Access Journals (Sweden)

    Tatiane Ohland

    2009-03-01

    Full Text Available O objetivo do presente trabalho foi avaliar a ação do AIB e cianamida hidrogenada no enraizamento de estacas apicais lenhosas de figueira 'Roxo de Valinhos'. Estacas caulinares lenhosas da porção apical dos ramos, coletadas no final da primeira quinzena de julho, foram padronizadas com 20 cm de comprimento e diâmetro próximo a sete mm. As estacas foram tratada ou não com AIB a 2.000 mg L-1 por 10 seg. e, em seguida, foram enterradas em leito de areia umedecido sob telado constituído de sombrite com 50% de luminosidade. Imediatamente após o plantio, cinco cm do ápice das estacas foram pincelados, com diferentes concentrações de cianamida hidrogenada: 0; 5; 10; 15; 20 e 25 mL L-1. Passados 60 dias da estaquia, foram mensurados a porcentagem de estacas vivas, enraizadas, brotadas, o número médio das brotações e raízes, além do comprimento médio das brotações. Uma amostragem de cada tratamento foi transplantada para sacolas plásticas com capacidade de 3 L (30 x 18 cm, preenchidas com substrato à base de casca de pínus e foram desbrotadas, preservando apenas uma única brotação por estaca. Aos 30; 60 e 90 dias após o transplantio, mensurou-se o comprimento médio da brotação. Para a melhoria do enraizamento adventícios, emissão e crescimento das brotações em estacas lenhosas apicais de figueira, devem-se aplicar 2.000 mg L-1 de AIB associados com 10 mL L-1 de cianamida hidrogenada.The objective of the present work was to verify the action of IBA and hydrogen cyanamide in the rooting of fig tree apical cuttings 'Roxo de Valinhos'. Woody cutting of apical portion was collected in the end of first fifteen days of July, standardized with 20 cm of length and seven millimeters of diameter. The cutting was treated or not with 2000 mg L-1 of IBA for 10 seconds. Soon after, the cuttings were buried in bed of sand humidified in nursery conditions with 50% of brightness. Immediately after the plantation, five cm of the apex of

  7. 高温和单氰胺对油桃休眠花芽呼吸代谢的影响%Effects of high temperature and hydrogen cyanamide on dormant nectarine' s floral bud respiratory metabolism

    Institute of Scientific and Technical Information of China (English)

    谭钺; 冷传远; 李玲; 徐臣善; 陈修德; 高东升

    2012-01-01

    以3年生盆栽‘曙光’油桃为材料,研究油桃自然休眠过程中50℃高温和单氰胺对花芽呼吸代谢的影响.结果表明:高温和单氰胺均可以打破油桃的自然休眠,导致休眠花芽呼吸代谢显著下降,其呼吸代谢的衰减可持续数小时.主要呼吸途径三羧酸循环(TCA)和磷酸戊糖途径(PPP)的运行均受到影响.未经破眠处理的花芽TCA和PPP均呈衰减趋势,而高温和单氰胺诱导了早期呼吸衰减结束后PPP的迅速活化.高温还表现出对TCA恢复的诱导,而单氰胺在96 h内未表现出这种作用.在高温和单氰胺打破自然休眠的机制中,呼吸衰减和随后出现的PPP活化可能是重要的组成部分.%Taking 3-year old potted ' Shuguang' nectarine (Prunus persica var. nectariana cv. Shuguang) as test material, this paper studied the effects of high temperature (50℃ , HT) and hydrogen cyanamide (HC) on the floral bud respiratory metabolism of the tree during its natural dormancy. Both HT and HC could break the natural dormancy of the tree, and lead to a significant decrease in the respiratory metabolism of floral buds for several hours. The main respiratory pathways, tricarboxylic acid cycle (TCA) and pentose phosphate pathway (PPP) , were affected. For the buds not received dormancy-breaking treatments, both the TCA and the PPP decreased, while treating with HT and HC induced a rapid recovery of PPP after the early respiratory attenuation. HT also induced the recovery of TCA, but HC did not show this effect in 96 hours. Therefore, respiratory attenuation and the following PPP activation could be the important part in the floral bud respiratory mechanism of HT- and HC-induced dormancy release.

  8. Effects of Hydrogen Cyanamide on the Floral Morphogenesis of Kiwifruit Buds Efectos de la Cianamida de Hidrógeno sobre la Morfogénesis Floral de Kiwi

    Directory of Open Access Journals (Sweden)

    Hakan Engin

    2010-09-01

    Full Text Available The influence of hydrogen cyanamide (HC on the flower bud development of kiwifruit (Actinidia deliciosa (A. Chev. C.F. Liang & A.R. Ferguson. ‘Hayward’ was studied. The bud samples were taken every 5-10 d starting from dormant season (March and fixed in FAA (10% formalin, 50% ethanol, 5% glacial acetic acid. Flower bud development was compared in three HC concentrations and the control. 1%, 2%, and 3% of HC was applied 35 d before the expected natural bud break. During the onset of bud break, only 57.6% of control buds had sepal primordia developed. On the other hand, HC treated buds had almost completed their stamen formation and started stigma primordia. When the control vines were in advanced bud break, gynoecial plateau already began to form in the vines treated with 2 and 3% HC. Vines treated with 1% HC lagged a little behind and had not started developing the gynoecial plateau. As the bud developed from the open cluster to the tight bud stage, the differences between the control and HC treated plants were more distinct. However, there were no differences between HC treatments as the ovule initiation took place in the buds.El presente estudio evalúa la influencia de la aplicación de cianamida de hidrogeno (HC sobre el desarrollo de las yemas florales de kiwi (Actinidia deliciosa (A. Chev. C.F. Liang & A.R. Ferguson cv. Hayward. Las muestras de yemas se tomaron cada 5-10 días comenzando en la época de dormancia en marzo y se fijaron en FAA (10% formaldehido, 50% etanol, 5% ácido acético glacial. Se comparó el desarrollo de las yemas florales en tres concentraciones de HC y el control. Se aplicó HC al 1%, 2% y 3% 35 días antes del brote natural de las yemas. En el momento de la apertura de las yemas, sólo el 57,6% de las yemas de control habían desarrollado los primordios de los sépalos. Por el contrario, las yemas tratadas con HC casi habían completado la formación de estambres y habían empezado el desarrollo de primordios

  9. Low-energy electron scattering from cyanamide

    Science.gov (United States)

    Wang, Kedong; Guo, Shuangcheng; Meng, Ju; Huang, Xiaotian; Wang, Yongfeng

    2016-09-01

    The low-energy electron collisions with cyanamide molecule are investigated by using the UK molecular R -matrix codes for electron energies ranging from 0.01 eV to 10 eV. Three models including static-exchange, static-exchange plus polarization, and close-coupling (CC) approximations are employed to reveal the dynamic interaction. Elastic (integrated and differential), momentum-transfer, and excitation cross sections from the ground state to the three low-lying electron excited states have been presented. Two shape resonances, two core-excited resonances, and two Feshbach resonances are detected in the CC approximation. The role of active space in the target and scattering problem including the resonances is discussed. The precise resonance parameters are found to be sensitive to the treatment of polarization effects employed. These resonances may be responsible for the fragments observed in a recent experiment of the dissociative electron attachments to cyanamide. Since the cyanamide molecule has a large permanent dipole moment, a Born closure procedure is used to account for the contribution of partial waves higher than l =4 to obtain converged cross sections.

  10. Amineborane Based Chemical Hydrogen Storage - Final Report

    International Nuclear Information System (INIS)

    The development of efficient and safe methods for hydrogen storage is a major hurdle that must be overcome to enable the use of hydrogen as an alternative energy carrier. The objectives of this project in the DOE Center of Excellence in Chemical Hydride Storage were both to develop new methods for on-demand, low temperature hydrogen release from chemical hydrides and to design high-conversion off-board methods for chemical hydride regeneration. Because of their reactive protic (N-H) and hydridic (B-H) hydrogens and high hydrogen contents, amineboranes such as ammonia borane, NH3BH3 (AB), 19.6-wt% H2, and ammonia triborane NH3B3H7 (AT), 17.7-wt% H2, were initially identified by the Center as promising, high-capacity chemical hydrogen storage materials with the potential to store and deliver molecular hydrogen through dehydrogenation and hydrolysis reactions. In collaboration with other Center partners, the Penn project focused both on new methods to induce amineborane H2-release and on new strategies for the regeneration the amineborane spent-fuel materials. The Penn approach to improving amineborane H2-release focused on the use of ionic liquids, base additives and metal catalysts to activate AB dehydrogenation and these studies successfully demonstrated that in ionic liquids the AB induction period that had been observed in the solid-state was eliminated and both the rate and extent of AB H2-release were significantly increased. These results have clearly shown that, while improvements are still necessary, many of these systems have the potential to achieve DOE hydrogen-storage goals. The high extent of their H2-release, the tunability of both their H2 materials weight-percents and release rates, and their product control that is attained by either trapping or suppressing unwanted volatile side products, such as borazine, continue to make AB/ionic-liquid based systems attractive candidates for chemical hydrogen storage applications. These studies also demonstrated

  11. Amineborane Based Chemical Hydrogen Storage - Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Sneddon, Larry G.

    2011-04-21

    The development of efficient and safe methods for hydrogen storage is a major hurdle that must be overcome to enable the use of hydrogen as an alternative energy carrier. The objectives of this project in the DOE Center of Excellence in Chemical Hydride Storage were both to develop new methods for on-demand, low temperature hydrogen release from chemical hydrides and to design high-conversion off-board methods for chemical hydride regeneration. Because of their reactive protic (N-H) and hydridic (B-H) hydrogens and high hydrogen contents, amineboranes such as ammonia borane, NH3BH3 (AB), 19.6-wt% H2, and ammonia triborane NH3B3H7 (AT), 17.7-wt% H2, were initially identified by the Center as promising, high-capacity chemical hydrogen storage materials with the potential to store and deliver molecular hydrogen through dehydrogenation and hydrolysis reactions. In collaboration with other Center partners, the Penn project focused both on new methods to induce amineborane H2-release and on new strategies for the regeneration the amineborane spent-fuel materials. The Penn approach to improving amineborane H2-release focused on the use of ionic liquids, base additives and metal catalysts to activate AB dehydrogenation and these studies successfully demonstrated that in ionic liquids the AB induction period that had been observed in the solid-state was eliminated and both the rate and extent of AB H2-release were significantly increased. These results have clearly shown that, while improvements are still necessary, many of these systems have the potential to achieve DOE hydrogen-storage goals. The high extent of their H2­-release, the tunability of both their H2 materials weight-percents and release rates, and their product control that is attained by either trapping or suppressing unwanted volatile side products, such as borazine, continue to make AB/ionic­-liquid based systems attractive candidates for chemical hydrogen storage applications. These studies also

  12. Use of hydrogen within a chemical Verbund

    Energy Technology Data Exchange (ETDEWEB)

    Blankertz, H.J.; Gall, M. [BASF SE, Ludwigshafen (Germany)

    2010-12-30

    Hydrogen is an essential building block within the value chains of chemical Verbund sites, even though it is not a product targeted within the sales portfolio of a chemical company. At most sites not only Hydrogen, but also the other products of a Synthesisgas plant - Carbonmonoxide and Oxogas (mixture of Hydrogen and Carbonmonoxide) - are needed as well. A predominant portion of the plants within a Verbund depends on its supply. So within a chemical Verbund the challenge is to supply these gases in varying load situations, utilize respective co-produced gases from other plants and do so with highest availability and flexibility. As storage of substantial gas quantities is not economically feasible, buffer capacity is very limited. This makes these gas supply networks very stiff, which means that every change within the system causes immediate effect. Transportation of gases in large volumes via road or rail is economically not feasible, therefore the gases supply of a Verbund site is a customized local set-up. For newly developed demand it has to be evaluated whether an own investment or purchase of respective gas quantities (dedicated plant or supply via pipeline operated by gas companies) is the most economic concept. Future challenges will be limited availability of conventional liquid and gaseous fossil feedstocks, still increasing demand especially in Asia and effects caused by regulations and consumer behaviour related to sustainability and environmental aspects. We will need new, improved and proven technologies to manage these challenges. (Published in summary form only) (orig.)

  13. Low energy electron attachment to cyanamide (NH2CN)

    International Nuclear Information System (INIS)

    Cyanamide (NH2CN) is a molecule relevant for interstellar chemistry and the chemical evolution of life. In the present investigation, dissociative electron attachment to NH2CN has been studied in a crossed electron–molecular beams experiment in the electron energy range from about 0 eV to 14 eV. The following anionic species were detected: NHCN−, NCN−, CN−, NH2−, NH−, and CH2−. The anion formation proceeds within two broad electron energy regions, one between about 0.5 and 4.5 eV and a second between 4.5 and 12 eV. A discussion of possible reaction channels for all measured negative ions is provided. The experimental results are compared with calculations of the thermochemical thresholds of the anions observed. For the dehydrogenated parent anion, we explain the deviation between the experimental appearance energy of the anion with the calculated corresponding reaction threshold by electron attachment to the isomeric form of NH2CN—carbodiimide

  14. Rational design of carbon nitride photocatalysts by identification of cyanamide defects as catalytically relevant sites

    Science.gov (United States)

    Lau, Vincent Wing-Hei; Moudrakovski, Igor; Botari, Tiago; Weinberger, Simon; Mesch, Maria B.; Duppel, Viola; Senker, Jürgen; Blum, Volker; Lotsch, Bettina V.

    2016-07-01

    The heptazine-based polymer melon (also known as graphitic carbon nitride, g-C3N4) is a promising photocatalyst for hydrogen evolution. Nonetheless, attempts to improve its inherently low activity are rarely based on rational approaches because of a lack of fundamental understanding of its mechanistic operation. Here we employ molecular heptazine-based model catalysts to identify the cyanamide moiety as a photocatalytically relevant `defect'. We exploit this knowledge for the rational design of a carbon nitride polymer populated with cyanamide groups, yielding a material with 12 and 16 times the hydrogen evolution rate and apparent quantum efficiency (400 nm), respectively, compared with the unmodified melon. Computational modelling and material characterization suggest that this moiety improves coordination (and, in turn, charge transfer kinetics) to the platinum co-catalyst and enhances the separation of the photogenerated charge carriers. The demonstrated knowledge transfer for rational catalyst design presented here provides the conceptual framework for engineering high-performance heptazine-based photocatalysts.

  15. Chemical equilibrium analysis of dry hydrogen combustion

    International Nuclear Information System (INIS)

    The present work is based on a thermo-chemical equilibrium model for studying the effect of combustion of hydrogen during postulated accident scenarios in nuclear reactor containments. This model is based on the method of element potentials which seeks to minimize the free energy of the system. The condition on internal energy balance is imposed as a constraint during the minimization process. Another simplified model purely based on the internal energy balance has also been implemented to investigate the isolated impact of free energy and the conditions under which it becomes dominant. The two models have been used to extract final pressures for a wide range of initial conditions and mixture compositions that are typically found during accident scenarios. In the absence of hydrogen combustion experimental data, such models will become important for laying down a first estimate on the possible outcomes. (author)

  16. Galactic chemical evolution hydrogen through zinc

    CERN Document Server

    Timmes, F X; Timmes, F X; Woosley, S E

    1994-01-01

    Using the output from a grid of 60 Type II supernova models (Woosley \\& Weaver 1994) of varying mass (11 \\ltaprx M/M\\sun \\ltaprx 40) and metallicity (0, 10^{-4}, 0.01, 0.1, and 1 Z\\sol), the chemical evolution of 76 stable isotopes, from hydrogen to zinc, is calculated. The chemical evolution calculation employs a simple dynamical model for the Galaxy (infall with a 4 billion year e-folding time scale onto a exponential disk and 1/r^2 bulge), and standard evolution parameters, such as a Salpeter initial mass function and a quadratic Schmidt star formation rate. The theoretical results are compared in detail with observed stellar abundances in stars with metallicities in the range -3.0 \\ltaprx [Fe/H] \\ltaprx 0.0 dex. While our discussion focuses on the solar neighborhood where there are the most observations, the supernovae rates, an intrinsically Galactic quantity, are also discussed.

  17. Chemical storage of hydrogen in few-layer graphene.

    Science.gov (United States)

    Subrahmanyam, K S; Kumar, Prashant; Maitra, Urmimala; Govindaraj, A; Hembram, K P S S; Waghmare, Umesh V; Rao, C N R

    2011-02-15

    Birch reduction of few-layer graphene samples gives rise to hydrogenated samples containing up to 5 wt % of hydrogen. Spectroscopic studies reveal the presence of sp(3) C-H bonds in the hydrogenated graphenes. They, however, decompose readily on heating to 500 °C or on irradiation with UV or laser radiation releasing all the hydrogen, thereby demonstrating the possible use of few-layer graphene for chemical storage of hydrogen. First-principles calculations throw light on the mechanism of dehydrogenation that appears to involve a significant reconstruction and relaxation of the lattice. PMID:21282617

  18. Chemical storage of hydrogen in few-layer graphene

    OpenAIRE

    Subrahmanyam, K. S.; Kumar, Prashant; Maitra, Urmimala; Govindaraj, A.; Hembram, K.P.S.S.; Waghmare, Umesh V.; RAO, C. N. R.

    2011-01-01

    Birch reduction of few-layer graphene samples gives rise to hydrogenated samples containing up to 5 wt % of hydrogen. Spectroscopic studies reveal the presence of sp3 C-H bonds in the hydrogenated graphenes. They, however, decompose readily on heating to 500 °C or on irradiation with UV or laser radiation releasing all the hydrogen, thereby demonstrating the possible use of few-layer graphene for chemical storage of hydrogen. First-principles calculations throw light on the mechanism of dehyd...

  19. [Effect of cyanamide on the level of endogenous ethanol in the liver of normal rats and in hypocorticism].

    Science.gov (United States)

    Tarasov, Iu A; Satanovskaia, V I; Shishkin, S N; Ostrovskiĭ, Iu M

    1988-01-01

    The rat liver endogenous ethanol level was found to increase under inhibition of aldehyde dehydrogenases by cyanamide. Adrenalectomy results in a decrease of the liver endogenous ethanol content and abolishes cyanamide effect on this index. One of the mechanisms of cyanamide toxic effect may be accumulation of different aldehydes including acetaldehyde.

  20. Effects of single cyanamide dose on free amino acid pool in rat brain

    Energy Technology Data Exchange (ETDEWEB)

    Ostrovskiy, S.Yu.

    Outbred rats were employed in trials on the effects of cyanamide - an inhibitor of aldehyde dehydrogenase proposed for the treatment of alcoholism - on the brain pool of essential and nonessential amino acid. Cyanamide was administered intraperitoneally in a dose of 60 mg/kg, followed in some experiments by intraperitoneal ethanol in a dose of 0.5 g/kg. Following cyanamide administration, marked enhancement of the levels of taurine, cystine, and GABA was noted, whereas the increase in serine was less pronounced. Cyanamide administration also induced depression of alanine, valine, leucine, phenylalanine, and of ethanolamine levels. Administration of ethanol after priming with cyanamide had only the additional effect of diminishing the levels of cysteic acid and ornithine in the brain. However, the differences between the cyanamide animals and the cyanamide + ethanol animals were not significant. With currently available data, it is difficult to tell whether the effects of cyanamide are due to elevation in acetaldehyde levels, or to some direct effect of the drug on protein or amino acid metabolism. 24 references.

  1. Proceedings of the DOE chemical energy storage and hydrogen energy systems contracts review

    Energy Technology Data Exchange (ETDEWEB)

    1980-02-01

    Sessions were held on electrolysis-based hydrogen storage systems, hydrogen production, hydrogen storage systems, hydrogen storage materials, end-use applications and system studies, chemical heat pump/chemical energy storage systems, systems studies and assessment, thermochemical hydrogen production cycles, advanced production concepts, and containment materials. (LHK)

  2. Inhibitory efficacy of calcium cyanamide on the pathogens of replant diseases in strawberry

    Institute of Scientific and Technical Information of China (English)

    WANG Lijing; HU Tongle; JI Lijing; CAO Keqiang

    2007-01-01

    Replant diseases in strawberry caused by Rhizoctonia solani,Fusarium oxysporum and Verticillium dahliae are serious problems for its sustainable production under continuous cropping.This research studied the inhibitory effect of calcium cyanamide on pathogenic fungi in Petri dishes and on sterilized soil.Results indicated that calcium cyanamide had an obvious inhibitory effect on three pathogens on potato dextrose agar (PDA) plates.Among them,the inhibitory effect on Rhizoctonia solani was the highest.As the concentrations of calcium cyanamide was increased from 0.1 to 10 mg/mL,the inhibition rate on mycelial growth increased from -1.43% to 100%.Inhibitory effects on Fusarium oxysporum and Verticillium dahliae also existed on Petri dishes but to a lesser extent.Similar results were also observed in sterilized soil.When the concentration of calcium cyanamide in sterilized soil was 0.1%,the inhibitory effect on Fusarium oxysporum and Verticillium dahliae was 68.46% and 54.46%,respectively.The inhibitive effect of calcium cyanamide on Fusariurn oxysporum and Verticillium dahliae increased quickly as the soil moisture changed from 10% to 40% for Verticillium dahliae and from 10% to 60% forFusarium oxysporum.This indicated that the inhibitive effect of calcium cyanamide could be influenced greatly by the moisture content in the soil.

  3. Non-precious metal catalysts prepared from precursor comprising cyanamide

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Hoon Taek; Zelenay, Piotr

    2015-10-27

    Catalyst comprising graphitic carbon and methods of making thereof; said graphitic carbon comprising a metal species, a nitrogen-containing species and a sulfur containing species. A catalyst for oxygen reduction reaction for an alkaline fuel cell was prepared by heating a mixture of cyanamide, carbon black, and a salt selected from an iron sulfate salt and an iron acetate salt at a temperature of from about 700.degree. C. to about 1100.degree. C. under an inert atmosphere. Afterward, the mixture was treated with sulfuric acid at elevated temperature to remove acid soluble components, and the resultant mixture was heated again under an inert atmosphere at the same temperature as the first heat treatment step.

  4. Down Select Report of Chemical Hydrogen Storage Materials, Catalysts, and Spent Fuel Regeneration Processes - May 2008

    Energy Technology Data Exchange (ETDEWEB)

    Ott, Kevin C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Linehan, Sue [Rohm and Haas, Philadelphia, PA (United States); Lipiecki, Frank [Rohm and Haas, Philadelphia, PA (United States); Christopher, Aardahl L. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2008-05-12

    Chemical Hydrogen Storage Center of Excellence FY2008 Second Quarter Milestone Report: Technical report describing assessment of hydrogen storage materials and progress towards meeting DOE’s hydrogen storage targets.

  5. Chemical Hydride Slurry for Hydrogen Production and Storage

    Energy Technology Data Exchange (ETDEWEB)

    McClaine, Andrew W

    2008-09-30

    The purpose of this project was to investigate and evaluate the attractiveness of using a magnesium chemical hydride slurry as a hydrogen storage, delivery, and production medium for automobiles. To fully evaluate the potential for magnesium hydride slurry to act as a carrier of hydrogen, potential slurry compositions, potential hydrogen release techniques, and the processes (and their costs) that will be used to recycle the byproducts back to a high hydrogen content slurry were evaluated. A 75% MgH2 slurry was demonstrated, which was just short of the 76% goal. This slurry is pumpable and storable for months at a time at room temperature and pressure conditions and it has the consistency of paint. Two techniques were demonstrated for reacting the slurry with water to release hydrogen. The first technique was a continuous mixing process that was tested for several hours at a time and demonstrated operation without external heat addition. Further work will be required to reduce this design to a reliable, robust system. The second technique was a semi-continuous process. It was demonstrated on a 2 kWh scale. This system operated continuously and reliably for hours at a time, including starts and stops. This process could be readily reduced to practice for commercial applications. The processes and costs associated with recycling the byproducts of the water/slurry reaction were also evaluated. This included recovering and recycling the oils of the slurry, reforming the magnesium hydroxide and magnesium oxide byproduct to magnesium metal, hydriding the magnesium metal with hydrogen to form magnesium hydride, and preparing the slurry. We found that the SOM process, under development by Boston University, offers the lowest cost alternative for producing and recycling the slurry. Using the H2A framework, a total cost of production, delivery, and distribution of $4.50/kg of hydrogen delivered or $4.50/gge was determined. Experiments performed at Boston

  6. Chemical Hydride Slurry for Hydrogen Production and Storage

    Energy Technology Data Exchange (ETDEWEB)

    McClaine, Andrew W

    2008-09-30

    The purpose of this project was to investigate and evaluate the attractiveness of using a magnesium chemical hydride slurry as a hydrogen storage, delivery, and production medium for automobiles. To fully evaluate the potential for magnesium hydride slurry to act as a carrier of hydrogen, potential slurry compositions, potential hydrogen release techniques, and the processes (and their costs) that will be used to recycle the byproducts back to a high hydrogen content slurry were evaluated. A 75% MgH2 slurry was demonstrated, which was just short of the 76% goal. This slurry is pumpable and storable for months at a time at room temperature and pressure conditions and it has the consistency of paint. Two techniques were demonstrated for reacting the slurry with water to release hydrogen. The first technique was a continuous mixing process that was tested for several hours at a time and demonstrated operation without external heat addition. Further work will be required to reduce this design to a reliable, robust system. The second technique was a semi-continuous process. It was demonstrated on a 2 kWh scale. This system operated continuously and reliably for hours at a time, including starts and stops. This process could be readily reduced to practice for commercial applications. The processes and costs associated with recycling the byproducts of the water/slurry reaction were also evaluated. This included recovering and recycling the oils of the slurry, reforming the magnesium hydroxide and magnesium oxide byproduct to magnesium metal, hydriding the magnesium metal with hydrogen to form magnesium hydride, and preparing the slurry. We found that the SOM process, under development by Boston University, offers the lowest cost alternative for producing and recycling the slurry. Using the H2A framework, a total cost of production, delivery, and distribution of $4.50/kg of hydrogen delivered or $4.50/gge was determined. Experiments performed at Boston

  7. Down Select Report of Chemical Hydrogen Storage Materials, Catalysts, and Spent Fuel Regeneration Processes

    Energy Technology Data Exchange (ETDEWEB)

    Ott, Kevin; Linehan, Sue; Lipiecki, Frank; Aardahl, Christopher L.

    2008-08-24

    The DOE Hydrogen Storage Program is focused on identifying and developing viable hydrogen storage systems for onboard vehicular applications. The program funds exploratory research directed at identifying new materials and concepts for storage of hydrogen having high gravimetric and volumetric capacities that have the potential to meet long term technical targets for onboard storage. Approaches currently being examined are reversible metal hydride storage materials, reversible hydrogen sorption systems, and chemical hydrogen storage systems. The latter approach concerns materials that release hydrogen in endothermic or exothermic chemical bond-breaking processes. To regenerate the spent fuels arising from hydrogen release from such materials, chemical processes must be employed. These chemical regeneration processes are envisioned to occur offboard the vehicle.

  8. Chemical kinetic performance losses for a hydrogen laser thermal thruster

    Science.gov (United States)

    Mccay, T. D.; Dexter, C. E.

    1985-01-01

    Projected requirements for efficient, economical, orbit-raising propulsion systems have generated investigations into several potentially high specific impulse, moderate thrust, advanced systems. One of these systems, laser thermal propulsion, utilizes a high temperature plasma as the enthalpy source. The plasma is sustained by a focused laser beam which maintains the plasma temperature at levels near 20,000 K. Since such temperature levels lead to total dissociation and high ionization, the plasma thruster system potentially has a high specific impulse decrement due to recombination losses. The nozzle flow is expected to be sufficiently nonequilibrium to warrant concern over the achievable specific impluse. This investigation was an attempt at evaluation of those losses. The One-Dimensional Kinetics (ODK) option of the Two-Dimensional Kinetics (TDK) Computer Program was used with a chemical kinetics rate set obtained from available literature to determine the chemical kinetic energy losses for typical plasma thruster conditions. The rates were varied about the nominal accepted values to band the possible losses. Kinetic losses were shown to be highly significant for a laser thermal thruster using hydrogen. A 30 percent reduction in specific impulse is possible simply due to the inability to completely extract the molecular recombination energy.

  9. Some recent efforts in chemical hydrogen storage at Loa Alamos

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, John C [Los Alamos National Laboratory; Davis, Benjamin L [Los Alamos National Laboratory; Burrell, Anthony K [Los Alamos National Laboratory; Nakagawa, Tessui [Los Alamos National Laboratory; Ott, Kevin C [Los Alamos National Laboratory; Smythe, Nathan C [Los Alamos National Laboratory; Sutton, Andrew D [Los Alamos National Laboratory; Henson, Neil J [Los Alamos National Laboratory; Baker, R. Thomas [U. OTTAWA; Hamilton, Charles W [OD VISION, INC.; Dixon, David A [U. ALABAMA; Garner Ill, Edward B [U. ALABAMA; Vasiliu, Monica [U. ALABAMA

    2010-12-08

    Within the transportation sector, a necessity towards realizing the use of hydrogen (H{sub 2}) as an alternative fuel, is its storage for controlled delivery. The U.S. DOE's Centers of Excellence (CoE) in H{sub 2} storage have pursued different methodologies (metal hydrides, chemical hydrides, and sorbents), for the express purpose of supplanting gasoline's current > 300 mile driving range. Chemical H{sub 2} storage has been dominated by one material, ammonia borane (H3B-NH3, AB), due to its high gravimetric capacity of H{sub 2} (19.6 wt %) and low molecular weight (30.7 g mol{sup -1} ). As such, a number of publications have described H{sub 2} release from amine boranes, yielding various rates depending on the method applied. The viability of any storage system is also dependent on efficient recyclability. Within our CoE we have thus endeavored to find efficient base-metal catalyzed AB dehydrogenation pathways and regeneration schemes for the spent fuel from H{sub 2} depleted AB. We will present some recent results in these areas in this vein.

  10. 76 FR 64022 - Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting

    Science.gov (United States)

    2011-10-17

    ... rule (December 1, 1993, 58 FR 63500). Hydrogen sulfide was listed under the criteria of EPCRA section... EPCRA section 313(d)(2)(B) (see 59 FR 61432, 61433, 61440-61442). Hydrogen sulfide has also been... adding hydrogen sulfide to the EPCRA section 313 list of toxic chemicals (58 FR 63500) (effective...

  11. Effect of chemical potential on the computer simulation of hydrogen storage in single walled carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    ZHENG Hong; WANG Shaoqing; CHENG Huiming

    2004-01-01

    Grand canonical Monte Carlo molecular simulations were carried out for hydrogen adsorption in single-walled carbon nanotubes. It was found that variations in chemical potential may result in a great change in the hydrogen storage capacity of single-walled carbon nanotubes. Hydrogen adsorption isotherms of single-walled carbon nanotubes at 298.15 K were calculated using a modified chemical potential, and the result obtained is closer to the experimental results. By comparing the experimental and simulation results, it is proposed that chemical adsorption may exist for hydrogen adsorption in single-walled carbon nanotubes.

  12. Catalytic hydrogenation reactors for the fine chemicals industries. Their design and operation.

    OpenAIRE

    Westerterp, K.R.; Molga, E.J.; Gelder, van, M.

    1997-01-01

    The design and operation of reactors for catalytic, hydrogenation in the fine chemical industries are discussed. The requirements for a good multiproduct catalytic hydrogenation unit as well as the choice of the reactor type are considered. Packed bed bubble column reactors operated without hydrogen recycle are recommended as the best choice to obtain a flexible reactor with good selectivities. The results of an experimental study of the catalytic hydrogenation of 2,4-dinitrotoluene in a mini...

  13. Analysis of hydrogen mobility in Nb-based alloy membranes in view of new description of hydrogen permeability based on hydrogen chemical potential

    Energy Technology Data Exchange (ETDEWEB)

    Suzuki, A. [Department of Materials Science and Engineering, Graduate School of Engineering, Nagoya University, Furo-Cho, Chikusa-ku, Nagoya 464-8603 (Japan); Yukawa, H., E-mail: hiroshi@nagoya-u.jp [Department of Materials Science and Engineering, Graduate School of Engineering, Nagoya University, Furo-Cho, Chikusa-ku, Nagoya 464-8603 (Japan); Nambu, T. [Department of Materials Science and Engineering, Suzuka National College of Technology, Shiroko-Cho, Mie 510-0294 (Japan); Matsumoto, Y. [Department of Mechanical Engineering, Oita National College of Technology, Maki, Oita 870-0152 (Japan); Murata, Y. [Department of Materials Science and Engineering, Graduate School of Engineering, Nagoya University, Furo-Cho, Chikusa-ku, Nagoya 464-8603 (Japan)

    2015-10-05

    Highlights: • The alloying effects on the mobility of hydrogen atom, B, in Nb have been investigated. • The analysis based on the new description of hydrogen permeation has been performed. • The mobility of hydrogen atom is expressed in a format of the Arrhenius equation. • The logarithm of the pre-exponential factor and the activation energy decrease linearly by alloying. • Ru, W and Mo in Nb enhance the hydrogen diffusivity at low temperature below T{sub int}. - Abstract: Hydrogen permeability of Nb-based alloy membranes have been analyzed in view of the new description of hydrogen permeation based on hydrogen chemical potential in order to investigate the alloying effects on the mobility of hydrogen atom, B. There is a liner relationship between the normalized hydrogen flux, J⋅L, and the PCT factor, f{sub PCT}. The mobility of hydrogen atom is expressed in a format of the Arrhenius equation. Then, the alloying effects on the activation energy, E, and the pre-exponential factor, B{sub 0}, have been investigated. It is found that logarithm of the pre-exponential factor, ln B{sub 0}, is proportional to the activation energy, E. In other words, when one factor decreases by alloying, the other factor also decreases linearly. As a result, the addition of ruthenium, tungsten and molybdenum into niobium enhances the hydrogen diffusivity at low temperature below the intersection temperature, T{sub int}.

  14. Hydrazine Borane and Hydrazinidoboranes as Chemical Hydrogen Storage Materials

    Directory of Open Access Journals (Sweden)

    Romain Moury

    2015-04-01

    Full Text Available Hydrazine borane N2H4BH3 and alkali derivatives (i.e., lithium, sodium and potassium hydrazinidoboranes MN2H3BH3 with M = Li, Na and K have been considered as potential chemical hydrogen storage materials. They belong to the family of boron- and nitrogen-based materials and the present article aims at providing a timely review while focusing on fundamentals so that their effective potential in the field could be appreciated. It stands out that, on the one hand, hydrazine borane, in aqueous solution, would be suitable for full dehydrogenation in hydrolytic conditions; the most attractive feature is the possibility to dehydrogenate, in addition to the BH3 group, the N2H4 moiety in the presence of an active and selective metal-based catalyst but for which further improvements are still necessary. However, the thermolytic dehydrogenation of hydrazine borane should be avoided because of the evolution of significant amounts of hydrazine and the formation of a shock-sensitive solid residue upon heating at >300 °C. On the other hand, the alkali hydrazinidoboranes, obtained by reaction of hydrazine borane with alkali hydrides, would be more suitable to thermolytic dehydrogenation, with improved properties in comparison to the parent borane. All of these aspects are surveyed herein and put into perspective.

  15. Environmental Problems From Tea Cultivation in Japan and a Control Measure Using Calcium Cyanamide

    Institute of Scientific and Technical Information of China (English)

    K.OH; T.KATO; LI Zhong-Pei; LI Fa-Yun

    2006-01-01

    A field experiment, involving lime N (calcium cyanamide, CaCN2) fertilization as a control measure, was conducted to study environmental problems induced by long-term heavy N application in Japanese tea fields. Long-term tea cultivation caused serious soil acidification. Seventy-seven percent of the 70 tea fields investigated had soil pH values below 4.0, and9% below 3.0, with the lowest value of 2.7. Moreover, excess N application in tea fields put a threat to plant growth,induced serious nitrate contamination to local water, and caused high nitrous oxide loss. Compared with the conventional high N application treatment (1 100 kg N ha-1) without lime N, the low N application (400 kg N ha-1) with calcium cyanamide effectively stopped soil acidification as well as achieved the same or slightly higher levels in tea yield and in total N and amino acid contents of tea shoots. The application of calcium cyanamide could be a suitable fertilization for the prevention of environmental problems in tea cultivation.

  16. LANL Virtual Center for Chemical Hydrogen Storage: Chemical Hydrogen Storage Using Ultra-high Surface Area Main Group Materials

    Energy Technology Data Exchange (ETDEWEB)

    Susan M. Kauzlarich; Phillip P. Power; Doinita Neiner; Alex Pickering; Eric Rivard; Bobby Ellis, T. M.; Atkins, A. Merrill; R. Wolf; Julia Wang

    2010-09-05

    The focus of the project was to design and synthesize light element compounds and nanomaterials that will reversibly store molecular hydrogen for hydrogen storage materials. The primary targets investigated during the last year were amine and hydrogen terminated silicon (Si) nanoparticles, Si alloyed with lighter elements (carbon (C) and boron (B)) and boron nanoparticles. The large surface area of nanoparticles should facilitate a favorable weight to volume ratio, while the low molecular weight elements such as B, nitrogen (N), and Si exist in a variety of inexpensive and readily available precursors. Furthermore, small NPs of Si are nontoxic and non-corrosive. Insights gained from these studies will be applied toward the design and synthesis of hydrogen storage materials that meet the DOE 2010 hydrogen storage targets: cost, hydrogen capacity and reversibility. Two primary routes were explored for the production of nanoparticles smaller than 10 nm in diameter. The first was the reduction of the elemental halides to achieve nanomaterials with chloride surface termination that could subsequently be replaced with amine or hydrogen. The second was the reaction of alkali metal Si or Si alloys with ammonium halides to produce hydrogen capped nanomaterials. These materials were characterized via X-ray powder diffraction, TEM, FTIR, TG/DSC, and NMR spectroscopy.

  17. Photoluminescence of amorphous carbon films fabricated by layer-by-layer hydrogen plasma chemical annealing method

    Institute of Scientific and Technical Information of China (English)

    徐骏; 黄晓辉; 李伟; 王立; 陈坤基

    2002-01-01

    A method in which nanometre-thick film deposition was alternated with hydrogen plasma annealing (layer-by-layermethod) was applied to fabricate hydrogenated amorphous carbon films in a conventional plasma-enhanced chemicalvapour deposition system. It was found that the hydrogen plasma treatment could decrease the hydrogen concentrationin the films and change the sp2/sp3 ratio to some extent by chemical etching. Blue photoluminescence was observed atroom temperature, as a result of the reduction of sp2 clusters in the films.

  18. Hydrogen production employing Spirulina maxima 2342: A chemical analysis

    Energy Technology Data Exchange (ETDEWEB)

    Juantorena, A.U.; Santoyo, E.; Gamboa, S.A.; Lastres, O.D. [Centro de Investigacion en Energia, UNAM, Temixco 62580, Morelos (Mexico); Sebastian, P.J. [Centro de Investigacion en Energia, UNAM, Temixco 62580, Morelos (Mexico); Cuerpo Academico de Energia, UP Chiapas, Tuxtla Gutierrez, Chiapas (Mexico); Sanchez-Escamilla, D. [Instituto de Investigaciones Electricas, Cuernavaca, Morelos (Mexico); Bustos, A. [Centro de Ciencias Fisicas, UNAM, Ave. Universidad, Cuernavaca, Morelos (Mexico); Eapen, D. [Investigacion y Desarrollo en Agroindustria, UP Chiapas, Tuxtla Gutierrez, Chiapas (Mexico)

    2007-10-15

    The biomass of the cyanobacteria, Spirulina maxima 2342, was autotrophically obtained in a 20 l bioreactor under illumination and air bubbling and analyzed for its photobiological hydrogen production capability. A volume of 250 ml of Spirulina sp. taken from the reactor was used as culture sample for performing the experiments. An illumination-agitation process was employed to induce the hydrogen photoproduction reaction. The hydrogen produced in this process was quantified by gas chromatography technique using Molesieve 5 A(16ft x (1)/(8)in) column and a thermal conductivity detector (with a detector temperature of 110{sup o}C and a column temperature of 60{sup o}C). The culture samples were finally observed in an electron microscope to evaluate the effect of vacuum on the Spirulina sp. cells. (author)

  19. Effect of chemical treatments on hydrogen storage behaviors of multi-walled carbon nanotubes

    International Nuclear Information System (INIS)

    In this work, the hydrogen storage behaviors of chemically treated multi-walled carbon nanotubes (MWNTs) were investigated. The surface properties of the functionalized MWNTs were confirmed by Fourier transfer infrared spectroscopy, X-ray diffraction, the Boehm titration method, and zeta-potential measurements. The hydrogen storage capacity of the MWNTs was evaluated at 298 K and 100 bar. In the experimental results, it was found that the chemical treatments introduced functional groups onto the MWNT surfaces. The amount of hydrogen storage was enhanced, by acidic surface treatment, to 0.42 wt.% in the acidic-treated MWNTs compared with 0.26 wt.% in the as-received MWNTs. Meanwhile, the basic surface treatment actually reduced the hydrogen storage capacity, to 0.24 wt.% in the basic-treated MWNTs sample. Consequently, it could be concluded that hydrogen storage is greatly influenced by the acidic characteristics of MWNT surfaces, resulting in enhanced electron acceptor-donor interaction at interfaces.

  20. Note: Dissolved hydrogen detection in power transformer oil based on chemically etched fiber Bragg grating.

    Science.gov (United States)

    Jiang, Jun; Ma, Guo-ming; Song, Hong-tu; Zhou, Hong-yang; Li, Cheng-rong; Luo, Ying-ting; Wang, Hong-bin

    2015-10-01

    A fiber Bragg grating (FBG) sensor based on chemically etched cladding to detect dissolved hydrogen is proposed and studied in this paper. Low hydrogen concentration tests have been carried out in mixed gases and transformer oil to investigate the repeatability and sensitivity. Moreover, to estimate the influence of etched cladding thickness, a physical model of FBG-based hydrogen sensor is analyzed. Experimental results prove that thin cladding chemically etched by HF acid solution improves the response to hydrogen detection in oil effectively. At last, the sensitivity of FBG sensor chemically etched 16 μm could be as high as 0.060 pm/(μl/l), increased by more than 30% in comparison to un-etched FBG. PMID:26521000

  1. Isotope effects on chemical shifts in the study of intramolecular hydrogen bonds

    DEFF Research Database (Denmark)

    Hansen, Poul Erik

    2015-01-01

    The paper deals with the use of isotope effects on chemical shifts in characterizing intramolecular hydrogen bonds. Both so-called resonance-assisted (RAHB) and non-RAHB systems are treated. The importance of RAHB will be discussed. Another very important issue is the borderline between “static......” and tautomeric systems. Isotope effects on chemical shifts are particularly useful in such studies. All kinds of intramolecular hydrogen bonded systems will be treated, typical hydrogen bond donors: OH, NH, SH and NH+, typical acceptors C=O, C=N, C=S C=N−. The paper will be deal with both secondary...... and primary isotope effects on chemical shifts. These two types of isotope effects monitor the same hydrogen bond, but from different angles...

  2. Isotope effects on chemical shifts in the study of intramolecular hydrogen bonds

    DEFF Research Database (Denmark)

    Hansen, Poul Erik

    2015-01-01

    The paper deals with the use of isotope effects on chemical shifts in characterizing intramolecular hydrogen bonds. Both so-called resonance-assisted (RAHB) and non-RAHB systems are treated. The importance of RAHB will be discussed. Another very important issue is the borderline between “static......” and tautomeric systems. Isotope effects on chemical shifts are particularly useful in such studies. All kinds of intramolecular hydrogen bonded systems will be treated, typical hydrogen bond donors: OH, NH, SH and NH+, typical acceptors C=O, C=N, C=S C=N−. The paper will be deal with both secondary and primary...... isotope effects on chemical shifts. These two types of isotope effects monitor the same hydrogen bond, but from different angles...

  3. Thermodynamic Feasibility of Hydrogen-Rich Gas Production Supported by Iron Based Chemical Looping Process

    Directory of Open Access Journals (Sweden)

    Grzegorz Słowiński

    2016-01-01

    Full Text Available The continuously increasing oil prices as well as stronger environmental regulations regarding greenhouse emissions made the greatest economic powers search a new, price competitive, and environment friendly energy carrier, such as hydrogen. The world research activities in these terms focus on the development of integrated hydrogen and power generating technologies, particularly technologies of hydrogen production from various carbonaceous resources, like methane, coal, biomass, or waste, often combined with carbon dioxide capture. In the paper the thermodynamic analysis of the enhancement of hydrogen production in iron based chemical looping process is presented. In this method, iron oxide is first reduced to iron with a reducing agent, such as carbon oxide, hydrogen, or mixture of both gases (synthesis gas, and then, in the inverse reaction with steam, it is regenerated to iron oxide, and pure stream of hydrogen is produced.

  4. Methods of controlling hydrogen fluoride pressure during chemical fabrication processes

    Science.gov (United States)

    Solovyov, Vyacheslav; Wiesmann, Harold

    2009-11-24

    The present invention is a method for producing a crystalline end-product. The method comprising exposing a fluoride-containing precursor to a hydrogen fluoride absorber under conditions suitable for the conversion of the precursor into the crystalline end-product.

  5. Chemical Reactions and Kinetics of the Carbon Monoxide Coupling in the Presence of Hydrogen

    Institute of Scientific and Technical Information of China (English)

    Fandong Meng; Genhui Xu; Zhenhua Li; Pa Du

    2002-01-01

    The chemical reactions and kinetics of the catalytic coupling reaction of carbon monoxide to diethyl oxalate were studied in the presence of hydrogen over a supported palladium catalyst in the gaseous phase at the typical coupling reaction conditions. The experiments were performed in a continuous flow fixed-bed reactor. The results indicated that hydrogen only reacts with ethyl nitrite to form ethanol, and kinetic studies revealed that the rate-determining step is the surface reaction of adsorbed hydrogen and the ethoxy radical (EtO-). A kinetic model is proposed and a comparison of the observed and calculated conversions showed that the rate expressions are of rather high confidence.

  6. Catalyst for Gas Phase Hydrogenation of Aldehydes Successfully Developed by Daqing Chemical Research Center

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    @@ A national invention patent has been granted to the method for preparation of the Cu-Zn-Al system catalyst for gas phase hydrogenation of aldehydes developed by the Daqing Chemi-cal Research Center (DCRC) under the PetroChina Petro-chemical Research Institute. This technology is mainly ap-plied to the gas phase process for hydrogenation of butanal/crotonaldehyde to manufacture butanol/octanol and has brought about hundreds of million RMB of economic ben-efits since its application.

  7. Hydrogen and chemicals production by plasma reforming methane

    International Nuclear Information System (INIS)

    Low temperature plasmas have excellent potential as on board transportation reformers for fuel cells. Because of their low temperature operation, they start up and shut down rapidly, and little energy is lost in waste heat that cannot easily be recovered from high temperature processes. Their use of electricity to drive reactions certainly requires good efficiency, but may simplify on-board systems. Partial oxidation has been shown to operate effectively as has steam reforming under these conditions. Hydrogen, COx, and C2s are the primary products of plasma reforming of methane. In this paper, the major reaction pathways and the results of the partial oxidation and steam reforming of methane will be discussed. (author)

  8. Hydrogen generation via photoelectrochemical water splitting using chemically exfoliated MoS2 layers

    International Nuclear Information System (INIS)

    Study on hydrogen generation has been of huge interest due to increasing demand for new energy sources. Photoelectrochemical reaction by catalysts was proposed as a promising technique for hydrogen generation. Herein, we report the hydrogen generation via photoelectrochecmial reaction using films of exfoliated 2-dimensional (2D) MoS2, which acts as an efficient photocatalyst. The film of chemically exfoliated MoS2 layers was employed for water splitting, leading to hydrogen generation. The amount of hydrogen was qualitatively monitored by observing overpressure of a water container. The high photo-current generated by MoS2 film resulted in hydrogen evolution. Our work shows that 2D MoS2 is one of the promising candidates as a photocatalyst for light-induced hydrogen generation. High photoelectrocatalytic efficiency of the 2D MoS2 shows a new way toward hydrogen generation, which is one of the renewable energy sources. The efficient photoelectrocatalytic property of the 2D MoS2 is possibly due to availability of catalytically active edge sites together with minimal stacking that favors the electron transfer

  9. Hydrogen generation via photoelectrochemical water splitting using chemically exfoliated MoS2 layers

    Directory of Open Access Journals (Sweden)

    R. K. Joshi

    2016-01-01

    Full Text Available Study on hydrogen generation has been of huge interest due to increasing demand for new energy sources. Photoelectrochemical reaction by catalysts was proposed as a promising technique for hydrogen generation. Herein, we report the hydrogen generation via photoelectrochecmial reaction using films of exfoliated 2-dimensional (2D MoS2, which acts as an efficient photocatalyst. The film of chemically exfoliated MoS2 layers was employed for water splitting, leading to hydrogen generation. The amount of hydrogen was qualitatively monitored by observing overpressure of a water container. The high photo-current generated by MoS2 film resulted in hydrogen evolution. Our work shows that 2D MoS2 is one of the promising candidates as a photocatalyst for light-induced hydrogen generation. High photoelectrocatalytic efficiency of the 2D MoS2 shows a new way toward hydrogen generation, which is one of the renewable energy sources. The efficient photoelectrocatalytic property of the 2D MoS2 is possibly due to availability of catalytically active edge sites together with minimal stacking that favors the electron transfer.

  10. Hydrogen generation via photoelectrochemical water splitting using chemically exfoliated MoS{sub 2} layers

    Energy Technology Data Exchange (ETDEWEB)

    Joshi, R. K., E-mail: r.joshi@unsw.edu.au, E-mail: alwarappan@cecri.res.in; Sahajwalla, V. [Centre for Sustainable Materials Research and Technology, School of Materials Science and Engineering, University of New South Wales, NSW 2052 (Australia); Shukla, S.; Saxena, S. [Department of Metallurgical Engineering and Materials Science, Indian Institute of Technology Bombay, Mumbai (India); Lee, G.-H. [Department of Material Science and Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of); Alwarappan, S., E-mail: r.joshi@unsw.edu.au, E-mail: alwarappan@cecri.res.in [CSIR-Central Electrochemical Research Institute, Karaikudi 630006, Tamilnadu (India)

    2016-01-15

    Study on hydrogen generation has been of huge interest due to increasing demand for new energy sources. Photoelectrochemical reaction by catalysts was proposed as a promising technique for hydrogen generation. Herein, we report the hydrogen generation via photoelectrochecmial reaction using films of exfoliated 2-dimensional (2D) MoS{sub 2}, which acts as an efficient photocatalyst. The film of chemically exfoliated MoS{sub 2} layers was employed for water splitting, leading to hydrogen generation. The amount of hydrogen was qualitatively monitored by observing overpressure of a water container. The high photo-current generated by MoS{sub 2} film resulted in hydrogen evolution. Our work shows that 2D MoS{sub 2} is one of the promising candidates as a photocatalyst for light-induced hydrogen generation. High photoelectrocatalytic efficiency of the 2D MoS{sub 2} shows a new way toward hydrogen generation, which is one of the renewable energy sources. The efficient photoelectrocatalytic property of the 2D MoS{sub 2} is possibly due to availability of catalytically active edge sites together with minimal stacking that favors the electron transfer.

  11. Hydrogen generation via photoelectrochemical water splitting using chemically exfoliated MoS2 layers

    Science.gov (United States)

    Joshi, R. K.; Shukla, S.; Saxena, S.; Lee, G.-H.; Sahajwalla, V.; Alwarappan, S.

    2016-01-01

    Study on hydrogen generation has been of huge interest due to increasing demand for new energy sources. Photoelectrochemical reaction by catalysts was proposed as a promising technique for hydrogen generation. Herein, we report the hydrogen generation via photoelectrochecmial reaction using films of exfoliated 2-dimensional (2D) MoS2, which acts as an efficient photocatalyst. The film of chemically exfoliated MoS2 layers was employed for water splitting, leading to hydrogen generation. The amount of hydrogen was qualitatively monitored by observing overpressure of a water container. The high photo-current generated by MoS2 film resulted in hydrogen evolution. Our work shows that 2D MoS2 is one of the promising candidates as a photocatalyst for light-induced hydrogen generation. High photoelectrocatalytic efficiency of the 2D MoS2 shows a new way toward hydrogen generation, which is one of the renewable energy sources. The efficient photoelectrocatalytic property of the 2D MoS2 is possibly due to availability of catalytically active edge sites together with minimal stacking that favors the electron transfer.

  12. Chemical bonding in hydrogen and lithium under pressure.

    Science.gov (United States)

    Naumov, Ivan I; Hemley, Russell J; Hoffmann, Roald; Ashcroft, N W

    2015-08-14

    Though hydrogen and lithium have been assigned a common column of the periodic table, their crystalline states under common conditions are drastically different: the former at temperatures where it is crystalline is a molecular insulator, whereas the latter is a metal that takes on simple structures. On compression, however, the two come to share some structural and other similarities associated with the insulator-to-metal and metal-to-insulator transitions, respectively. To gain a deeper understanding of differences and parallels in the behaviors of compressed hydrogen and lithium, we performed an ab initio comparative study of these systems in selected identical structures. Both elements undergo a continuous pressure-induced s-p electronic transition, though this is at a much earlier stage of development for H. The valence charge density accumulates in interstitial regions in Li but not in H in structures examined over the same range of compression. Moreover, the valence charge density distributions or electron localization functions for the same arrangement of atoms mirror each other as one proceeds from one element to the other. Application of the virial theorem shows that the kinetic and potential energies jump across the first-order phase transitions in H and Li are opposite in sign because of non-local effects in the Li pseudopotential. Finally, the common tendency of compressed H and Li to adopt three-fold coordinated structures as found is explained by the fact that such structures are capable of yielding a profound pseudogap in the electronic densities of states at the Fermi level, thereby reducing the kinetic energy. These results have implications for the phase diagrams of these elements and also for the search for new structures with novel properties. PMID:26277151

  13. Chemical bonding in hydrogen and lithium under pressure

    Energy Technology Data Exchange (ETDEWEB)

    Naumov, Ivan I.; Hemley, Russell J. [Geophysical Laboratory, Carnegie Institution of Washington, 5251 Broad Branch Rd. NW, Washington, DC 20015 (United States); Hoffmann, Roald [Baker Laboratory, Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853 (United States); Ashcroft, N. W. [Laboratory of Atomic and Solid State Physics and Cornell Center for Materials Research, Cornell University, Clark Hall, Ithaca, New York 14853 (United States)

    2015-08-14

    Though hydrogen and lithium have been assigned a common column of the periodic table, their crystalline states under common conditions are drastically different: the former at temperatures where it is crystalline is a molecular insulator, whereas the latter is a metal that takes on simple structures. On compression, however, the two come to share some structural and other similarities associated with the insulator-to-metal and metal-to-insulator transitions, respectively. To gain a deeper understanding of differences and parallels in the behaviors of compressed hydrogen and lithium, we performed an ab initio comparative study of these systems in selected identical structures. Both elements undergo a continuous pressure-induced s-p electronic transition, though this is at a much earlier stage of development for H. The valence charge density accumulates in interstitial regions in Li but not in H in structures examined over the same range of compression. Moreover, the valence charge density distributions or electron localization functions for the same arrangement of atoms mirror each other as one proceeds from one element to the other. Application of the virial theorem shows that the kinetic and potential energies jump across the first-order phase transitions in H and Li are opposite in sign because of non-local effects in the Li pseudopotential. Finally, the common tendency of compressed H and Li to adopt three-fold coordinated structures as found is explained by the fact that such structures are capable of yielding a profound pseudogap in the electronic densities of states at the Fermi level, thereby reducing the kinetic energy. These results have implications for the phase diagrams of these elements and also for the search for new structures with novel properties.

  14. Chemical bonding in hydrogen and lithium under pressure.

    Science.gov (United States)

    Naumov, Ivan I; Hemley, Russell J; Hoffmann, Roald; Ashcroft, N W

    2015-08-14

    Though hydrogen and lithium have been assigned a common column of the periodic table, their crystalline states under common conditions are drastically different: the former at temperatures where it is crystalline is a molecular insulator, whereas the latter is a metal that takes on simple structures. On compression, however, the two come to share some structural and other similarities associated with the insulator-to-metal and metal-to-insulator transitions, respectively. To gain a deeper understanding of differences and parallels in the behaviors of compressed hydrogen and lithium, we performed an ab initio comparative study of these systems in selected identical structures. Both elements undergo a continuous pressure-induced s-p electronic transition, though this is at a much earlier stage of development for H. The valence charge density accumulates in interstitial regions in Li but not in H in structures examined over the same range of compression. Moreover, the valence charge density distributions or electron localization functions for the same arrangement of atoms mirror each other as one proceeds from one element to the other. Application of the virial theorem shows that the kinetic and potential energies jump across the first-order phase transitions in H and Li are opposite in sign because of non-local effects in the Li pseudopotential. Finally, the common tendency of compressed H and Li to adopt three-fold coordinated structures as found is explained by the fact that such structures are capable of yielding a profound pseudogap in the electronic densities of states at the Fermi level, thereby reducing the kinetic energy. These results have implications for the phase diagrams of these elements and also for the search for new structures with novel properties.

  15. Synthesis and Engineering Materials Properties of Fluid Phase Chemical Hydrogen Storage Materials for Automotive Applications

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Young Joon; Westman, Matthew P.; Karkamkar, Abhijeet J.; Chun, Jaehun; Ronnebro, Ewa

    2015-09-01

    Among candidates for chemical hydrogen storage in PEM fuel cell automotive applications, ammonia borane (AB, NH3BH3) is considered to be one of the most promising materials due to its high practical hydrogen content of 14-16 wt%. This material is selected as a surrogate chemical for a hydrogen storage system. For easier transition to the existing infrastructure, a fluid phase hydrogen storage material is very attractive and thus, we investigated the engineering materials properties of AB in liquid carriers for a chemical hydrogen storage slurry system. Slurries composed of AB and high temperature liquids were prepared by mechanical milling and sonication in order to obtain stable and fluidic properties. Volumetric gas burette system was adopted to observe the kinetics of the H2 release reactions of the AB slurry and neat AB. Viscometry and microscopy were employed to further characterize slurries engineering properties. Using a tip-sonication method we have produced AB/silicone fluid slurries at solid loadings up to 40wt% (6.5wt% H2) with viscosities less than 500cP at 25°C.

  16. Quantum chemical simulation of hydrogen like states in silicon and diamond

    International Nuclear Information System (INIS)

    The quantum-chemical methods of the complete neglect of differential overlap (CNDO) and intermediate neglect of differential overlap (INDO) are used to calculate the electronic structure of atomic hydrogen (muonium) located at different interstital sites of the silicon and diamond crystal lattices. The electronic g- and hyperfine interaction tensors of the impure atom are determined.The results obtained are compared with the experimental data on the 'normal' (Mu') and 'anomalous' (Mu*) muonium centers as well as on the hydrogen-bearing Si-AA9 EPR center which is a hydrogen-bearing analogue of (Mu*). The most likely localization sites for hydrogen (muonium) atoms in silicon and diamond crystals are established. 22 refs

  17. Analysis of solar chemical processes for hydrogen production from water splitting thermochemical cycles

    International Nuclear Information System (INIS)

    This paper presents a process analysis of ZnO/Zn, Fe3O4/FeO and Fe2O3/Fe3O4 thermochemical cycles as potential high efficiency, large scale and environmentally attractive routes to produce hydrogen by concentrated solar energy. Mass and energy balances allowed estimation of the efficiency of solar thermal energy to hydrogen conversion for current process data, accounting for chemical conversion limitations. Then, the process was optimized by taking into account possible improvements in chemical conversion and heat recoveries. Coupling of the thermochemical process with a solar tower plant providing concentrated solar energy was considered to scale up the system. An economic assessment gave a hydrogen production cost of 7.98$ kg-1 and 14.75$ kg-1 of H2 for, respectively a 55 MWth and 11 MWth solar tower plant operating 40 years

  18. Study of filament performance in heat transfer and hydrogen dissociation in diamond chemical vapor deposition

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Hot-filament chemical vapor deposition (HFCVD) is a promising method for commercial production of diamond films.Filament performance in heat transfer and hydrogen decomposition in reactive environment was investigated. Power consumption by the filament in vacuum, helium and 2% CH4/H2 was experimentally determined in temperature range 1300℃-2200℃. Filament heat transfer mechanism in C-H reactive environment was calculated and analyzed. The result shows that due to surface carburization and slight carbon deposition, radiation in stead of hydrogen dissociation, becomes the largest contributor to power consumption. Filament-surface dissociation of H2 was observed at temperatures below 1873K, demonstrating the feasibility of diamond growth at low filament temperatures. The effective activation energies of hydrogen dissociation on several clean refractory filaments were derived from power consumption data in literatures. They are all lower than that of thermal dissociation of hydrogen, revealing the nature of catalytic dissociation of hydrogen on filament surface. Observation of substrate temperature suggested a weakerrole of atomic hydrogen recombination in heating substrates in C-H environment than in pure hydrogen.

  19. Chemical Bonding States of TiC Films before and after Hydrogen Ion Irradiation

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    TiC films deposited by rf magnetron sputtering followed by Ar+ ion bombardment were irradiated with a hydrogen ion beam. X-ray photoelectron spectroscopy (XPS) was used for characterization of the chemical bonding states of C and Ti elements of the TiC films before and after hydrogen ion irradiation, in order to understand the effect of hydrogen ion irradiation on the films and to study the mechanism of hydrogen resistance of TiC films. Conclusions can be drawn that ion bombardment at moderate energy can cause preferential physical sputtering of carbon atoms from the surface of low atomic number (Z) material. This means that ion beam bombardment leads to the formation of a non-stoichiometric composition of TiC on the surface.TiC films prepared by ion beam mixing have the more excellent characteristic of hydrogen resistance. One important cause, in addition to TiC itself, is that there are many vacant sites in TiC created by ion beam mixing.These defects can easily trap hydrogen and effectively enhance the effect of hydrogen resistance.

  20. High Pressure Chemical Vapor Deposition of Hydrogenated Amorphous Silicon Films and Solar Cells.

    Science.gov (United States)

    He, Rongrui; Day, Todd D; Sparks, Justin R; Sullivan, Nichole F; Badding, John V

    2016-07-01

    Thin films of hydrogenated amorphous silicon can be produced at MPa pressures from silane without the use of plasma at temperatures as low as 345 °C. High pressure chemical vapor deposition may open a new way to low cost deposition of amorphous silicon solar cells and other thin film structures over very large areas in very compact, simple reactors. PMID:27174318

  1. Chemical evolution of spiral galaxies: models with star formation proportional to molecular hydrogen

    OpenAIRE

    Tosi, M.; Angeles I. Díaz

    1990-01-01

    This is an electronic version of an article published in Monthly Notices of the Royal Astronomical Society. Tosi, M., Díaz, A.I. Chemical evolution of spiral galaxies: models with star formation proportional to molecular hydrogen. Monthly Notices of the Royal Astronomical Society 246 (1990): 616-623

  2. Lignin solubilization and aqueous phase reforming for the production of aromatic chemicals and hydrogen

    NARCIS (Netherlands)

    Zakzeski, J.; Weckhuysen, B.M.

    2011-01-01

    The solubilization and aqueous phase reforming of lignin, including kraft, soda, and alcell lignin along with sugarcane bagasse, at low temperatures (T≤498 K) and pressures (P≤29 bar) is reported for the first time for the production of aromatic chemicals and hydrogen. Analysis of lignin model compo

  3. The statistical shift of the chemical potential causing anomalous conductivity in hydrogenated microcrystalline silicon

    NARCIS (Netherlands)

    Lof, R.W.; Schropp, R.E.I.

    2010-01-01

    The behavior of the electrical conductivity in hydrogenated microcrystalline silicon (μ c-Si:H) that is frequently observed is explained by considering the statistical shift in the chemical potential as a function of the crystalline fraction (Xc), the dangling bond density (N db), and the doping den

  4. 75 FR 8889 - Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting

    Science.gov (United States)

    2010-02-26

    ... toxic chemicals as part of a 1993 final rule (December 1, 1993, 58 FR 63500). Hydrogen sulfide was... Federal Register of February 4, 1987 (52 FR 3479) to provide guidance regarding the recommended content... Federal Register of May 23, 1991 (56 FR 23703) regarding the recommended content of petitions to...

  5. Supercritical fluid chemical deposition of Pd nanoparticles on magnesium–scandium alloy for hydrogen storage

    Energy Technology Data Exchange (ETDEWEB)

    Couillaud, Samuel; Kirikova, Marina [CNRS, ICMCB, UPR 9048, F-33600 Pessac (France); Univ. Bordeaux, ICMCB, UPR 9048, F-33600 Pessac (France); Zaïdi, Warda; Bonnet, Jean-Pierre [LRCS, UMR CNRS 6007, 33 rue Saint-Leu, 80039-Amiens (France); Marre, Samuel; Aymonier, Cyril [CNRS, ICMCB, UPR 9048, F-33600 Pessac (France); Univ. Bordeaux, ICMCB, UPR 9048, F-33600 Pessac (France); Zhang, Junxian; Cuevas, Fermin; Latroche, Michel [ICMPE, CNRS-UPEC, UMR 7182, 2-8 rue Henri Dunant, 94320-Thiais (France); Aymard, Luc [LRCS, UMR CNRS 6007, 33 rue Saint-Leu, 80039-Amiens (France); Bobet, Jean-Louis, E-mail: bobet@icmcb-bordeaux.cnrs.fr [CNRS, ICMCB, UPR 9048, F-33600 Pessac (France); Univ. Bordeaux, ICMCB, UPR 9048, F-33600 Pessac (France)

    2013-10-15

    Highlights: •Nanoparticles of Pd were deposed on the binary compound Mg{sub 0.65}Sc{sub 0.35} using the Supercritical Fluid Chemical Deposition (SFCD) method. •Numerous parameters were tested and optimized in order to obtain a homogeneous deposition. •At the first step, Pd@Mg0.65Sc0.35 decomposes into ScH{sub 2} and MgH{sub 2} under hydrogen pressure (1 MPa) at 330 °C. •The mixture, after decomposition absorbs hydrogen reversibly on Mg/MgH{sub 2} couple with good kinetics. -- Abstract: The deposition of Pd nanoparticles on the binary compound Mg{sub 0.65}Sc{sub 0.35} using the Supercritical Fluid Chemical Deposition (SFCD) method was performed. There, the SFCD operating parameters (co-solvent, temperature, CO{sub 2} and hydrogen pressure, reaction time) have been optimized to obtain homogeneous deposition of Pd nanoparticles (around 10 nm). The hydrogenation properties of the optimized Pd@Mg{sub 0.65}Sc{sub 0.35} material were determined and compared to those of Mg{sub 0.65}Sc{sub 0.35}Pd{sub 0.024}. The latter compound forms at 300 °C and 1 MPa of H{sub 2} a hydride that crystallizes in the fluorite structure, absorbs reversibly 1.5 wt.% hydrogen and exhibits fast kinetics. In contrast, Pd@Mg{sub 0.65}Sc{sub 0.35} compound decomposes into ScH{sub 2} and MgH{sub 2} during hydrogen absorption under the same conditions. However, reversible sorption reaches 3.3 wt.% of hydrogen while keeping good kinetics. The possible roles of Pd on the hydrogen-induced alloy decomposition are discussed.

  6. Catalytic Hydrogenation of Bio-Oil for Chemicals and Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Elliott, Douglas C.

    2006-02-14

    The scope of work includes optimizing processing conditions and demonstrating catalyst lifetime for catalyst formulations that are readily scaleable to commercial operations. We use a bench-scale, continuous-flow, packed-bed, catalytic, tubular reactor, which can be operated in the range of 100-400 mL/hr., from 50-400 C and up to 20MPa (see Figure 1). With this unit we produce upgraded bio-oil from whole bio-oil or useful bio-oil fractions, specifically pyrolytic lignin. The product oils are fractionated, for example by distillation, for recovery of chemical product streams. Other products from our tests have been used in further testing in petroleum refining technology at UOP and fractionation for product recovery in our own lab. Further scale-up of the technology is envisioned and we will carry out or support process design efforts with industrial partners, such as UOP.

  7. The influence of hydrogen on the chemical, mechanical, optical/electronic, and electrical transport properties of amorphous hydrogenated boron carbide

    Science.gov (United States)

    Nordell, Bradley J.; Karki, Sudarshan; Nguyen, Thuong D.; Rulis, Paul; Caruso, A. N.; Purohit, Sudhaunshu S.; Li, Han; King, Sean W.; Dutta, Dhanadeep; Gidley, David; Lanford, William A.; Paquette, Michelle M.

    2015-07-01

    Because of its high electrical resistivity, low dielectric constant (κ), high thermal neutron capture cross section, and robust chemical, thermal, and mechanical properties, amorphous hydrogenated boron carbide (a-BxC:Hy) has garnered interest as a material for low-κ dielectric and solid-state neutron detection applications. Herein, we investigate the relationships between chemical structure (atomic concentration B, C, H, and O), physical/mechanical properties (density, porosity, hardness, and Young's modulus), electronic structure [band gap, Urbach energy (EU), and Tauc parameter (B1/2)], optical/dielectric properties (frequency-dependent dielectric constant), and electrical transport properties (resistivity and leakage current) through the analysis of a large series of a-BxC:Hy thin films grown by plasma-enhanced chemical vapor deposition from ortho-carborane. The resulting films exhibit a wide range of properties including H concentration from 10% to 45%, density from 0.9 to 2.3 g/cm3, Young's modulus from 10 to 340 GPa, band gap from 1.7 to 3.8 eV, Urbach energy from 0.1 to 0.7 eV, dielectric constant from 3.1 to 7.6, and electrical resistivity from 1010 to 1015 Ω cm. Hydrogen concentration is found to correlate directly with thin-film density, and both are used to map and explain the other material properties. Hardness and Young's modulus exhibit a direct power law relationship with density above ˜1.3 g/cm3 (or below ˜35% H), below which they plateau, providing evidence for a rigidity percolation threshold. An increase in band gap and decrease in dielectric constant with increasing H concentration are explained by a decrease in network connectivity as well as mass/electron density. An increase in disorder, as measured by the parameters EU and B1/2, with increasing H concentration is explained by the release of strain in the network and associated decrease in structural disorder. All of these correlations in a-BxC:Hy are found to be very similar to those

  8. Ozonation of refractory chemicals in leachate with hydrogen peroxide

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Nearly 97% of organic chemicals in Hong Kong leachatecould be effectively removed by the UASB(upflow anaerobic sludgeblanket) process followed by the Fenton coagulation. The COD ofleachate was lowered from an average of 12900 mg/L to 1440 mg/hafter the UASB treatment, and was further lowered to 394 mg/L afterthe Fenton coagulation. The remaining refractory residues could befurther removed by ozonation with the addition of H2O2. Theozonation for the supernatant of the Fenton coagulation was mosteffective at pH 7-8, with the addition of 300 mg/L of H2O2, and 30min of reaction. The final effluent contained only 85 mg/L of CODand l0 mg/L of BOD5. On the other hand, direct ozonation of UASBeffluent lowered the COD to 905 mg/L and BOD5 to l03 mg/L.Ozonation improved the biodegradability of the organic residues,and also converted part of organic-N in the leachate into NH3-N andNO3--N.

  9. Adsorption and dissociation of molecular hydrogen on Pt/CeO2 catalyst in the hydrogen spillover process: A quantum chemical molecular dynamics study

    International Nuclear Information System (INIS)

    Ultra accelerated quantum chemical molecular dynamics method (UA-QCMD) was used to study the dynamics of the hydrogen spillover process on Pt/CeO2 catalyst surface for the first time. The direct observation of dissociative adsorption of hydrogen on Pt/CeO2 catalyst surface as well as the diffusion of dissociative hydrogen from the Pt/CeO2 catalyst surface was simulated. The diffusion of the hydrogen atom in the gas phase explains the high reactivity observed in the hydrogen spillover process. Chemical changes, change of adsorption states and structural changes were investigated. It was observed that parallel adsorption of hydrogen facilitates the dissociative adsorption leading to hydrogen desorption. Impact with perpendicular adsorption of hydrogen causes the molecular adsorption on the surface, which decelerates the hydrogen spillover. The present study also indicates that the CeO2 support has strong interaction with Pt catalyst, which may cause an increase in Pt activity as well as enhancement of the metal catalyst dispersions and hence increasing the rate of hydrogen spillover reaction.

  10. Hydrogen dilution effect on microstructure of Si thin film grown by catalyzer enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    The effect of hydrogen dilution on microstructure of in situ polycrystalline Si (poly-Si) films grown by catalyzer-enhanced chemical vapor deposition (CECVD) has been investigated by using transmission electron microscopy (TEM) and transmission electron diffraction (TED) analysis. It was shown that the increase of the hydrogen dilution ratio resulted in transition of microstructure of Si thin film from amorphous to polycrystalline in CECVD at low substrate temperature (∼80 deg. C). These results indicate that the CECVD technique is a promising candidate to grow high-quality in situ polycrystalline Si films on glass or a flexible substrate for low-temperature poly-Si (LTPS) and flexible displays

  11. Hydrogen dilution effect on microstructure of Si thin film grown by catalyzer enhanced chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Han-Ki [School of Advanced Materials and Systems Engineering, Kumoh National Institute of Technology (KIT), 1 Yangho-dong, Gumi, Gyeongbuk, 730-701 (Korea, Republic of)]. E-mail: hkkim@kumoh.ac.kr

    2006-12-15

    The effect of hydrogen dilution on microstructure of in situ polycrystalline Si (poly-Si) films grown by catalyzer-enhanced chemical vapor deposition (CECVD) has been investigated by using transmission electron microscopy (TEM) and transmission electron diffraction (TED) analysis. It was shown that the increase of the hydrogen dilution ratio resulted in transition of microstructure of Si thin film from amorphous to polycrystalline in CECVD at low substrate temperature ({approx}80 deg. C). These results indicate that the CECVD technique is a promising candidate to grow high-quality in situ polycrystalline Si films on glass or a flexible substrate for low-temperature poly-Si (LTPS) and flexible displays.

  12. Chemical Hydrogen Storage Using Polyhedral Borane Anions and Aluminum-Ammonia-Borane Complexes

    Energy Technology Data Exchange (ETDEWEB)

    Hawthorne, M. Frederick; Jalisatgi, Satish S.; Safronov, Alexander V.; Lee, Han Beak; Wu, Jianguo

    2010-10-01

    Phase 1. Hydrolysis of borohydride compounds offer the potential for significant hydrogen storage capacity, but most work to date has focused on one particular anion, BH4-, which requires high pH for stability. Other borohydride compounds, in particular polyhedral borane anions offer comparable hydrogen storage capacity without requiring high pH media and their long term thermal and hydrolytic stability coupled with non-toxic nature make them a very attractive alternative to NaBH4. The University of Missouri project provided the overall program focal point for the investigation of catalytic hydrolysis of polyhedral borane anions for hydrogen release. Due to their inherent stability, a transition metal catalyst was necessary for the hydrolysis of polyhedral borane anions. Transition metal ions such as cobalt, nickel, palladium and rhodium were investigated for their catalytic activity in the hydrolysis of nido-KB11H14, closo-K2B10H10, and closo-K2B12H12. The rate of hydrolysis follows first-order kinetics with respect to the concentration of the polyhedral borane anion and surface area of the rhodium catalyst. The rate of hydrolysis depends upon a) choice of polyhedral borane anion, c) concentration of polyhedral borane anion, d) surface area of the rhodium catalyst and e) temperature of the reaction. In all cases the yield of hydrogen was 100% which corresponds to ~7 wt% of hydrogen (based on material wt%). Phase 2. The phase 2 of program at the University of Missouri was focused upon developing aluminum ammonia-boranes (Al-AB) as chemical hydrogen storage materials, specifically their synthesis and studies of their dehydrogenation. The ammonia borane molecule (AB) is a demonstrated source of chemically stored hydrogen (19.6 wt%) which meets DOE performance parameters except for its regeneration from spent AB and elemental hydrogen. The presence of an aluminum center bonded to multiple AB residues might combine the efficiency of AB dehydrogenation with an aluminum

  13. Synthesis and enhanced hydrogen desorption kinetics of magnesium hydride using hydriding chemical vapor synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jin-Ho [Icheon Branch, Korea Institute of Ceramic Engineering and Technology (KICET), Icheon-si, Gyeonggi-do (Korea, Republic of); Kim, Byung-Goan [Korea Energy Materials Co.Ltd., 409, Daegu Technopark, 1-11, Hosan-Dong, Dalse-Gu 704-230 (Korea, Republic of); Kang, Yong-Mook, E-mail: dake@kaist.ac.kr [Department of Chemistry, Dongguk University-Seoul, 100715 Seoul (Korea, Republic of)

    2012-07-15

    Highlights: Black-Right-Pointing-Pointer We synthesized pure MgH{sub 2} by a hydriding chemical vapor synthesis process in a hydrogen atmosphere. Black-Right-Pointing-Pointer The particle size HCVS-MgH{sub 2} was drastically reduced to the sub-micron or micrometer-scale. Black-Right-Pointing-Pointer HCVS-MgH{sub 2} showed different shapes (needle-like nanofibers and angulated plate) depending on the deposited position. Black-Right-Pointing-Pointer HCVS-MgH{sub 2} desorbed hydrogen up to about 7.2 wt% and 7.1 wt%. - Abstract: This paper describes the hydriding chemical vapor synthesis (HCVS) of the hydrogen storage alloy MgH{sub 2} in a hydrogen atmosphere and the product's hydrogenation properties. Mg powder was used as a starting material to produce submicron MgH{sub 2} and uniformly heated to a temperature of 600 Degree-Sign C for Mg vaporization. The effects of deposited positions in HCVS reactor on the morphology and the composition of the obtained products were examined by using X-ray diffraction (XRD), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) analyses. It is clearly seen that after the HCVS process, the particle size of synthesized MgH{sub 2} was drastically reduced to the sub-micron or micrometer-scale and these showed different shapes (needle-like nanofibers and angulated plate) depending on the deposited position. The hydrogen desorption temperatures of HCVS-MgH{sub 2} were measured using a differential scanning calorimeter (DSC). It was found that after the HCVS process, the desorption temperature of HCVS-MgH{sub 2} decreased from 430 to 385 Degree-Sign C and, simultaneously, the smallest particle size and the highest specific surface area were obtained. These observations indicate that the minimum hydrogen desorption temperature of HCVS-MgH{sub 2} powder with needle-like form can be obtained, and that this temperature is dependent on the particle size and the specific surface area of the products. The thermogravimetric

  14. Problems of application of porous silicon to chemical and photocatalytic production of hydrogen

    International Nuclear Information System (INIS)

    Advantages of the use of silicon and porous silicon (PS) for the chemical production of hydrogen have been analyzed and compared with other fuels. An analytic expression is derived for the dependence of the volume of hydrogen produced at the PS interaction with water on the material porosity, as well as for the corresponding energy yield, when the produced gas is used in the power sources of electronic systems. It is found that the silicon porosity growth results in a reduction of the total volume of hydrogen released in the reaction with water, as compared with the amount of H2 obtained from the initial quantity of raw silicon. This effect is explained by significant losses of a material at PS formation. The ratio between the accumulation of hydrogen in the PS material and silicon losses in the etchant is determined to be optimal for the silicon porosity in the interval of 60-70%. When applying the produced hydrogen in fuel cells, the etching of silicon provides a growth of the output power, but reduces the total amount of the produced energy. Those mechanisms are analyzed to demonstrate the inexpedience of using the composites on the basis of pure nano-PS for the photocatalytic water dissociation

  15. The influence of hydrogen on the chemical, mechanical, optical/electronic, and electrical transport properties of amorphous hydrogenated boron carbide

    Energy Technology Data Exchange (ETDEWEB)

    Nordell, Bradley J.; Karki, Sudarshan; Nguyen, Thuong D.; Rulis, Paul; Caruso, A. N.; Paquette, Michelle M., E-mail: paquettem@umkc.edu [Department of Physics and Astronomy, University of Missouri-Kansas City, Kansas City, Missouri 64110 (United States); Purohit, Sudhaunshu S. [Department of Chemistry, University of Missouri-Kansas City, Kansas City, Missouri 64110 (United States); Li, Han; King, Sean W. [Logic Technology Development, Intel Corporation, Hillsboro, Oregon 97124 (United States); Dutta, Dhanadeep; Gidley, David [Department of Physics, University of Michigan, Ann Arbor, Michigan 48109 (United States); Lanford, William A. [Department of Physics, University at Albany, Albany, New York 12222 (United States)

    2015-07-21

    Because of its high electrical resistivity, low dielectric constant (κ), high thermal neutron capture cross section, and robust chemical, thermal, and mechanical properties, amorphous hydrogenated boron carbide (a-B{sub x}C:H{sub y}) has garnered interest as a material for low-κ dielectric and solid-state neutron detection applications. Herein, we investigate the relationships between chemical structure (atomic concentration B, C, H, and O), physical/mechanical properties (density, porosity, hardness, and Young's modulus), electronic structure [band gap, Urbach energy (E{sub U}), and Tauc parameter (B{sup 1/2})], optical/dielectric properties (frequency-dependent dielectric constant), and electrical transport properties (resistivity and leakage current) through the analysis of a large series of a-B{sub x}C:H{sub y} thin films grown by plasma-enhanced chemical vapor deposition from ortho-carborane. The resulting films exhibit a wide range of properties including H concentration from 10% to 45%, density from 0.9 to 2.3 g/cm{sup 3}, Young's modulus from 10 to 340 GPa, band gap from 1.7 to 3.8 eV, Urbach energy from 0.1 to 0.7 eV, dielectric constant from 3.1 to 7.6, and electrical resistivity from 10{sup 10} to 10{sup 15} Ω cm. Hydrogen concentration is found to correlate directly with thin-film density, and both are used to map and explain the other material properties. Hardness and Young's modulus exhibit a direct power law relationship with density above ∼1.3 g/cm{sup 3} (or below ∼35% H), below which they plateau, providing evidence for a rigidity percolation threshold. An increase in band gap and decrease in dielectric constant with increasing H concentration are explained by a decrease in network connectivity as well as mass/electron density. An increase in disorder, as measured by the parameters E{sub U} and B{sup 1/2}, with increasing H concentration is explained by the release of strain in the network and associated decrease in

  16. 75 FR 19319 - Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting; Extension of Comment...

    Science.gov (United States)

    2010-04-14

    ... requirements for hydrogen sulfide (75 FR 8889). B. Why and for How Long Is EPA Extending the Comment Period... Number (CAS No.) 7783-06-4) (75 FR 8889). The purpose of today's action is to inform interested parties... AGENCY 40 CFR Part 372 RIN 2025-AA27 Hydrogen Sulfide; Community Right-to-Know Toxic Chemical...

  17. Preparation and reactivity towards hydrazines of bis(cyanamide) and bis(cyanoguanidine) complexes of the iron triad.

    Science.gov (United States)

    Albertin, Gabriele; Antoniutti, Stefano; Caia, Alfonso; Castro, Jesús

    2014-05-21

    Bis(diethylcyanamide) [Fe(N≡CNEt2)2L4](BPh4)2 1a and bis(cyanoguanidine) [Fe{N≡CN(H)C(NH2)=NH}2L4](BPh4)2 1b [L = P(OEt)3] complexes were prepared by allowing iron(II) chloride to react first with an excess of P(OEt)3 and then of the appropriate cyanamide, followed by addition of an excess of NaBPh4. Instead, bis(complexes) of ruthenium and osmium [M(N≡CNEt2)2L4](BPh4)2 2a, 3a and [M{N≡CN(H)C(NH2)=NH}2L4](BPh4)2 2b, 3b (M = Ru 2, Os 3) were prepared by reacting hydrides MH2L4 first with either triflic acid HOTf or methyltriflate MeOTf and then with an excess of the appropriate cyanamide. Hydride-diethylcyanamide [MH(N≡CNEt2)L4]BPh4 4a, 5a and hydride-cyanoguanidine complexes [MH{N≡CN(H)C(NH2)=NH}L4](BPh4)2 4b, 5b (M = Ru 4, Os 5) were also obtained by reacting MH2L4 first with one equivalent of HOTf or MeOTf and then with the appropriate cyanamide. Treatment of bis(cyanamide) and bis(cyanoguanidine) complexes 1-3 with hydrazines RNHNH2 afforded hydrazinecarboximidamide derivatives [M{η(2)-N(H)=C(NEt2)N(R)NH2}L4](BPh4)2 6a-12a and [M{η(2)-N(H)=C[N=C(NH2)2]N(R)NH2}L4](BPh4)2 6b-12b (M = Fe 6-8, Ru 9, 10, Os 11, 12; R = H 6, 9, 11, Me 7, 10, 12, Ph 8). A reaction path involving nucleophilic attack by hydrazine on the cyanamide carbon atom is proposed. All the complexes were characterised by spectroscopy and X-ray crystal structure determination of [Os{η(2)-NH=C[N=C(NH2)2]N(CH3)NH2}{P(OEt)3}4](BPh4)2 12b. PMID:24691705

  18. Optimizing the Binding Energy of Hydrogen on Nanostructured Carbon Materials through Structure Control and Chemical Doping

    Energy Technology Data Exchange (ETDEWEB)

    Jie Liu

    2011-02-01

    The DOE Hydrogen Sorption Center of Excellence (HSCoE) was formed in 2005 to develop materials for hydrogen storage systems to be used in light-duty vehicles. The HSCoE and two related centers of excellence were created as follow-on activities to the DOE Office of Energy Efficiency and Renewable Energy’s (EERE’s) Hydrogen Storage Grand Challenge Solicitation issued in FY 2003. The Hydrogen Sorption Center of Excellence (HSCoE) focuses on developing high-capacity sorbents with the goal to operate at temperatures and pressures approaching ambient and be efficiently and quickly charged in the tank with minimal energy requirements and penalties to the hydrogen fuel infrastructure. The work was directed at overcoming barriers to achieving DOE system goals and identifying pathways to meet the hydrogen storage system targets. To ensure that the development activities were performed as efficiently as possible, the HSCoE formed complementary, focused development clusters based on the following four sorption-based hydrogen storage mechanisms: 1. Physisorption on high specific surface area and nominally single element materials 2. Enhanced H2 binding in Substituted/heterogeneous materials 3. Strong and/or multiple H2 binding from coordinated but electronically unsatruated metal centers 4. Weak Chemisorption/Spillover. As a member of the team, our group at Duke studied the synthesis of various carbon-based materials, including carbon nanotubes and microporous carbon materials with controlled porosity. We worked closely with other team members to study the effect of pore size on the binding energy of hydrogen to the carbon –based materials. Our initial project focus was on the synthesis and purification of small diameter, single-walled carbon nanotubes (SWNTs) with well-controlled diameters for the study of their hydrogen storage properties as a function of diameters. We developed a chemical vapor deposition method that synthesized gram quantities of carbon nanotubes with

  19. Materials Engineering and Scale Up of Fluid Phase Chemical Hydrogen Storage for Automotive Applications

    Energy Technology Data Exchange (ETDEWEB)

    Westman, Matthew P.; Chun, Jaehun; Choi, Young Joon; Ronnebro, Ewa

    2016-01-25

    Among candidates for chemical hydrogen storage in PEM fuel cell automotive applications, ammonia borane (AB, NH3BH3) is considered to be one of the most promising materials due to its high hydrogen content of 14-16 wt% below 200°C and high volumetric density. In our previous paper, we selected AB in silicone oil as a role model for a slurry hydrogen storage system. Materials engineering properties were optimized by increasing solid loading by using an ultra-sonic process. In this paper, we proceeded to scale up to liter size batches with solid loadings up to 50 wt% (8 wt% H2) with dynamic viscosities less than 1000cP at 25°C. The use of a non-ionic surfactant, Triton X-15, shows significant promise in controlling the level of foaming produced during the thermal dehydrogenation of the AB. Through the development of new and efficient processing techniques and the ability to adequately control the foaming, stable homogenous slurries of high solid loading have been demonstrated as a viable hydrogen delivery source.

  20. Extent of hydrogen coverage of Si(001) under chemical vapor deposition conditions from ab initio approaches

    Science.gov (United States)

    Rosenow, Phil; Tonner, Ralf

    2016-05-01

    The extent of hydrogen coverage of the Si(001) c(4 × 2) surface in the presence of hydrogen gas has been studied with dispersion corrected density functional theory. Electronic energy contributions are well described using a hybrid functional. The temperature dependence of the coverage in thermodynamic equilibrium was studied computing the phonon spectrum in a supercell approach. As an approximation to these demanding computations, an interpolated phonon approach was found to give comparable accuracy. The simpler ab initio thermodynamic approach is not accurate enough for the system studied, even if corrections by the Einstein model for surface vibrations are considered. The on-set of H2 desorption from the fully hydrogenated surface is predicted to occur at temperatures around 750 K. Strong changes in hydrogen coverage are found between 1000 and 1200 K in good agreement with previous reflectance anisotropy spectroscopy experiments. These findings allow a rational choice for the surface state in the computational treatment of chemical reactions under typical metal organic vapor phase epitaxy conditions on Si(001).

  1. Chemical and Phase Evolution of Amorphous Molybdenum Sulfide Catalysts for Electrochemical Hydrogen Production.

    Science.gov (United States)

    Lee, Sang Chul; Benck, Jesse D; Tsai, Charlie; Park, Joonsuk; Koh, Ai Leen; Abild-Pedersen, Frank; Jaramillo, Thomas F; Sinclair, Robert

    2016-01-26

    Amorphous MoSx is a highly active, earth-abundant catalyst for the electrochemical hydrogen evolution reaction. Previous studies have revealed that this material initially has a composition of MoS3, but after electrochemical activation, the surface is reduced to form an active phase resembling MoS2 in composition and chemical state. However, structural changes in the MoSx catalyst and the mechanism of the activation process remain poorly understood. In this study, we employ transmission electron microscopy (TEM) to image amorphous MoSx catalysts activated under two hydrogen-rich conditions: ex situ in an electrochemical cell and in situ in an environmental TEM. For the first time, we directly observe the formation of crystalline domains in the MoSx catalyst after both activation procedures as well as spatially localized changes in the chemical state detected via electron energy loss spectroscopy. Using density functional theory calculations, we investigate the mechanisms for this phase transformation and find that the presence of hydrogen is critical for enabling the restructuring process. Our results suggest that the surface of the amorphous MoSx catalyst is dynamic: while the initial catalyst activation forms the primary active surface of amorphous MoS2, continued transformation to the crystalline phase during electrochemical operation could contribute to catalyst deactivation. These results have important implications for the application of this highly active electrocatalyst for sustainable H2 generation. PMID:26624225

  2. Surface characterization and chemical analysis of bamboo substrates pretreated by alkali hydrogen peroxide.

    Science.gov (United States)

    Song, Xueping; Jiang, Yan; Rong, Xianjian; Wei, Wei; Wang, Shuangfei; Nie, Shuangxi

    2016-09-01

    The surface characterization and chemical analysis of bamboo substrates by alkali hydrogen peroxide pretreatment (AHPP) were investigated in this study. The results tended to manifest that AHPP prior to enzymatic and chemical treatment was potential for improving accessibility and reactivity of bamboo substrates. The inorganic components, organic solvent extractives and acid-soluble lignin were effectively removed by AHPP. X-ray photoelectron spectroscopy (XPS) analysis indicated that the surface of bamboo chips had less lignin but more carbohydrate after pre-treatment. Fiber surfaces became etched and collapsed, and more pores and debris on the substrate surface were observed with Scanning Electron Microscopy (SEM). Brenauer-Emmett-Teller (BET) results showed that both of pore volume and surface area were increased after AHPP. Although XRD analysis showed that AHPP led to relatively higher crystallinity, pre-extraction could overall enhance the accessibility of enzymes and chemicals into the bamboo structure. PMID:27311789

  3. Middle atmosphere heating by exothermic chemical reactions involving odd-hydrogen species

    Science.gov (United States)

    Mlynczak, Martin G.; Solomon, Susan

    1991-01-01

    The rate of heating which occurs in the middle atmosphere due to four exothermic reactions involving members of the odd-hydrogen family is calculated. The following reactions are considered: O + OH yields O2 + H; H + O2 + M yields HO2 + M; H + O3 yields OH + O2; and O + HO2 yields OH + O2. It is shown that the heating rates due to these reactions rival the oxygen-related heating rates conventionally considered in middle-atmosphere models. The conversion of chemical potential energy into molecular translational energy (heat) by these odd-hydrogen reactions is shown to be a significant energy source in the middle atmosphere that has not been previously considered.

  4. Hydrogen Plasma Durability of Chemically Treated SnO2 Thin Films

    Science.gov (United States)

    Kawabata, Keishi; Tanaka, Takeshi; Hirose, Masataka

    1993-10-01

    The chemical stability of SnO2 surfaces against hydrogen plasma exposure has been studied by treating a SnO2/glass system either in steam at a substrate temperature of 200 and 400°C or in ethyl alcohol at 200 and 400°C, or by fluorinating the surface at 400°C in an NF3+O2 gas mixture. Also, an electroplated Zn layer on SnO2 has been oxidized at 400°C. X-ray photoelectron spectroscopy of such surfaces has revealed that the reduction reaction of the SnO2 surface exposed to hydrogen plasma is dramatically suppressed by the steam treatment at 400°C.

  5. THE IMPROVEMENT OF ELECTRON FIELD EMISSION FROM AMORPHOUS CARBON FILMS DUE TO HYDROGEN PLASMA CHEMICAL ANNEALING EFFECT

    Institute of Scientific and Technical Information of China (English)

    J. Xu; X.H. Huang; L. Wang; W. Li; K.J. Chen; J.B. Xu

    2001-01-01

    Hydrogenated amorphous carbon films were fabricated by using layer-by-layer deposi-tion method and hydrogen dilution method in a small d.c.-assisted plasma enhancedchemical vapor deposition system. It was found that the hydrogen plasma treatmentcould change the sp2/sp3 ratio to some extent by chemical etching. The improvementsof field emission characteristics were observed compared with that from conventionallydeposited a-C films, which can be attributed to the large field enhancement effect dueto the inhomogeneous distribution of nanometer scale sp2 clusters and the reductionof the surface emission barrier due to the hydrogen termination.

  6. Recombinant human diamine oxidase activity is not inhibited by ethanol, acetaldehyde, disulfiram, diethyldithiocarbamate or cyanamide.

    Science.gov (United States)

    Bartko, Johann; Gludovacz, Elisabeth; Petroczi, Karin; Borth, Nicole; Jilma, Bernd; Boehm, Thomas

    2016-08-01

    Human diamine oxidase (hDAO, EC 1.4.3.22) is the key enzyme in the degradation of extracellular histamine. Consumption of alcohol is a known trigger of mast cell degranulation in patients with mast cell activation syndrome. Ethanol may also interfere with enzymatic histamine degradation, but reports on the effects on DAO activity are controversial. There are also conflicting reports whether disulfiram, an FDA-approved agent in the treatment of alcohol dependence, inhibits DAO. We therefore investigated the inhibitory potential of ethanol and disulfiram and their metabolites on recombinant human DAO (rhDAO) in three different assay systems. Relevant concentrations of ethanol, acetaldehyde, and acetate did not inhibit rhDAO activity in an in vitro assay system using horseradish peroxidase (HRP) -mediated luminol oxidation. The aldehyde dehydrogenase (ALDH; EC 1.2.1.3) inhibitors cyanamide and its dimer dicyanamide also had no effect on DAO activity. In one assay system, the irreversible ALDH inhibitor disulfiram and its main metabolite diethyldithiocarbamate seemed to inhibit DAO activity. However, the decreased product formation was not due to a direct block of DAO activity but resulted from inhibition of peroxidase employed in the coupled system. Our in vitro data do not support a direct blocking effect of ethanol, disulfiram, and their metabolites on DAO activity in vivo. PMID:27401969

  7. An Integrated Photoelectrochemical-Chemical Loop for Solar-Driven Overall Splitting of Hydrogen Sulfide

    DEFF Research Database (Denmark)

    Zong, Xu; Han, Jingfeng; Seger, Brian;

    2014-01-01

    Abundant and toxic hydrogen sulfide (H2S) from industry and nature has been traditionally considered a liability. However, it represents a potential resource if valuable H-2 and elemental sulfur can be simultaneously extracted through a H2S splitting reaction. Herein a photochemical-chemical loop...... linked by redox couples such as Fe2+/Fe3+ and I-/I-3(-) for photoelectrochemical H-2 production and H2S chemical absorption redox reactions are reported. Using functionalized Si as photoelectrodes, H2S was successfully split into elemental sulfur and H-2 with high stability and selectivity under...... simulated solar light. This new conceptual design will not only provide a possible route for using solar energy to convert H2S into valuable resources, but also sheds light on some challenging photochemical reactions such as CH4 activation and CO2 reduction....

  8. Excitation of the aromatic infrared emission bands: Chemical energy in hydrogenated amorphous carbon particles?

    CERN Document Server

    Duley, Walter W

    2011-01-01

    We outline a model for the heating of hydrogenated amorphous (HAC) dust via the release of stored chemical energy and show that this energy (~12 kJ/mole) is sufficient to heat dust grains of classical size (50-1000 {\\AA}) to temperatures at which they can emit at 3.3 {\\mu}m and other "UIR" wavelengths. Using laboratory data, we show that this heating process is consistent with a concentration of a few percent of dangling bonds in HAC and may be initiated by the recombination of trapped H atoms. We suggest that the release of chemical energy from dust represents an additional source of excitation for the UIR bands relaxing the previous requirement that only stochastically heated molecules having fewer than ~ 50 atoms can produce emission at 3.3 {\\mu}m.

  9. Formation and Transport of Atomic Hydrogen in Hot-Filament Chemical Vapor Deposition Reactors

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    In this paper we focus on diamond film hot-filament chemical vapor deposition reactors where the only reactant ishydrogen so as to study the formation and transport of hydrogen atoms. Analysis of dimensionless numbers forheat and mass transfer reveals that thermal conduction and diffusion are the dominant mechanisms for gas-phaseheat and mass transfer, respectively. A simplified model has been established to simulate gas-phase temperature andH concentration distributions between the filament and the substrate. Examination of the relative importance ofhomogeneous and heterogeneous production of H atoms indicates that filament-surface decomposition of molecularhydrogen is the dominant source of H and gas-phase reaction plays a negligible role. The filament-surface dissociationrates of H2 for various filament temperatures were calculated to match H-atom concentrations observed in the liter-ature or derived from power consumption by filaments. Arrhenius plots of the filament-surface hydrogen dissociationrates suggest that dissociation of H2 at refractory filament surface is a catalytic process, which has a rather lowereffective activation energy than homogeneous thermal dissociation. Atomic hydrogen, acting as an important heattransfer medium to heat the substrate, can freely diffuse from the filament to the substrate without recombination.

  10. Acute toxic effect of calcium cyanamide on golden apple snail (Pomacea canaliculata).%石灰氮对福寿螺的急性毒性效应

    Institute of Scientific and Technical Information of China (English)

    赵本良; 章家恩; 代魏; 罗明珠; 宋春秀

    2011-01-01

    福寿螺(Pomacea canaliculata)是世界自然保护联盟认定的世界100种恶性外来入侵物种之一,在华南地区已对水稻生产造成严重危害.本研究将福寿螺按照壳高(H)分为小螺(5 mm≤H<15 mm)、中螺(15 mm≤H<25 mm)、大螺(25 mm≤H<35 mm)和超大螺(35 mm≤H<45 mm),通过室内毒性试验,探讨了化学肥料石灰氮(氰氨化钙)对不同体型福寿螺的毒性效应.结果表明:石灰氮对不同大小福寿螺毒性效应显著,尤其是对中小福寿螺具有很强的抑制和杀灭作用;石灰氮处理7 d后,最低浓度0.2 g·L-1处理造成71%死亡率,其他处理死亡率均在95%以上,其中3.0和5.0 g·L-1处理中福寿螺全部死亡;石灰氮对不同大小福寿螺的半抑制浓度(24 h)和半致死浓度(96 h)大小顺序均为小螺<中螺<大螺<超大螺;石灰氮对福寿螺的抑制效应显著,其对福寿螺的平均半抑制浓度为0.08~0.39 g·L-1;1.0和5.0 g·L-1浓度的石灰氮处理24 h后,福寿螺鳃组织SOD酶活性呈极显著下降,分别为对照的41%和60%.本研究表明,石灰氮在入侵生物福寿螺的防治方面有一定应用潜力,有望成为一种新型的"杀螺肥料".%Golden apple snail ( Pomacea canaliculata) is one of the 100 worst invasive alien species cognized by World Conservation Union, and has been resulting in a mass loss of rice production in South China. In this study, the snails according to their shell height ( H) were divided in to four groups, i. e. , small size (5 mm ≤ H<15 mm), medium size (15 mm ≤ H<25 mm), large size (25 mm≤H<35 mm) , and extra large size (35 mm≤ H<45 mm) , and a laboratory toxicity test was conducted to evaluate the molluscicidal activity of chemical fertilizer calcium cyanamide ( CaCN2) in controlling different sizes P. canaliculata. Calcium cyanamide had signifi cant molluscicidal effect on different sizes, especially small and medium sizes P. canaliculata. After treated one week, 0. 2 g

  11. Facile Gold-Catalyzed Heterocyclization of Terminal Alkynes and Cyanamides Leading to Substituted 2-Amino-1,3-Oxazoles.

    Science.gov (United States)

    Rassadin, Valentin A; Boyarskiy, Vadim P; Kukushkin, Vadim Yu

    2015-07-17

    Facile gold-catalyzed heterocyclization based upon intermolecular trapping of the generated α-oxo gold carbenes with various cyanamides R(2)R(3)NCN (R(2)/R(3) = Alk/Alk, -(CH2)2O(CH2)2-, Ar/Ar, Ar/H) has been developed. In most cases, 2-amino-1,3-oxazoles functionalized at the nitrogen atom as well as at the fifth position of the heterocyclic ring (12 examples) were isolated in good to moderate yields. PMID:26135038

  12. Effect of the hydrogen flow rate on the structural and optical properties of hydrogenated amorphous silicon thin films prepared by plasma enhanced chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Ben Amor, Sana; Dimassi, Wissem; Ali Tebai, Mohamed; Ezzaouia, Hatem [Photovoltaic Laboratory Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia)

    2012-10-15

    Hydrogenated amorphous silicon (a-Si:H) thin films were deposited from pure silane (SiH{sub 4}) and hydrogen (H{sub 2}) gas mixture by plasma enhanced chemical vapor deposition (PECVD) method at low temperature (400 C) using high rf power (60 W). The structural and optical properties of these films are systematically investigated as a function of the flow rate of hydrogen (F{sub H2}).The surface morphology is analyzed by atomic force microscopy (AFM). The characterization of these films with low angle X-ray diffraction revealed that the crystallite size in the films tends to decrease with increase in (F{sub H2}). The Fourier transform infrared (FTIR) spectroscopic analysis showed that at low values of (F{sub H2}),the hydrogen bonding in Si:H films shifts from di-hydrogen (Si-H{sub 2}) and (Si-H{sub 2})n complexes to the mono-hydrogen (Si-H) bonding configuration. Finally, for these optimized conditions, the deposition rate decreases with increasing (F{sub H2}). (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  13. Hydrogen

    OpenAIRE

    John O’M. Bockris

    2011-01-01

    The idea of a “Hydrogen Economy” is that carbon containing fuels should be replaced by hydrogen, thus eliminating air pollution and growth of CO2 in the atmosphere. However, storage of a gas, its transport and reconversion to electricity doubles the cost of H2 from the electrolyzer. Methanol made with CO2 from the atmosphere is a zero carbon fuel created from inexhaustible components from the atmosphere. Extensive work on the splitting of water by bacteria shows that if wastes are used as the...

  14. An Experimental and Chemical Kinetics Study of the Combustion of Syngas and High Hydrogen Content Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Santoro, Robers [Pennsylvania State Univ., State College, PA (United States); Dryer, Frederick [Princeton Univ., NJ (United States); Ju, Yiguang [Princeton Univ., NJ (United States)

    2013-09-30

    An integrated and collaborative effort involving experiments and complementary chemical kinetic modeling investigated the effects of significant concentrations of water and CO2 and minor contaminant species (methane [CH4], ethane [C2H6], NOX, etc.) on the ignition and combustion of HHC fuels. The research effort specifically addressed broadening the experimental data base for ignition delay, burning rate, and oxidation kinetics at high pressures, and further refinement of chemical kinetic models so as to develop compositional specifications related to the above major and minor species. The foundation for the chemical kinetic modeling was the well validated mechanism for hydrogen and carbon monoxide developed over the last 25 years by Professor Frederick Dryer and his co-workers at Princeton University. This research furthered advance the understanding needed to develop practical guidelines for realistic composition limits and operating characteristics for HHC fuels. A suite of experiments was utilized that that involved a high-pressure laminar flow reactor, a pressure-release type high-pressure combustion chamber and a high-pressure turbulent flow reactor.

  15. Hydrogen-free spray pyrolysis chemical vapor deposition method for the carbon nanotube growth: Parametric studies

    Energy Technology Data Exchange (ETDEWEB)

    Ionescu, Mihnea Ioan; Zhang Yong; Li Ruying [Department of Mechanical and Materials Engineering, University of Western Ontario, London, ON. N6A 5B9 (Canada); Sun Xueliang, E-mail: xsun@eng.uwo.ca [Department of Mechanical and Materials Engineering, University of Western Ontario, London, ON. N6A 5B9 (Canada); Abou-Rachid, Hakima; Lussier, Louis-Simon [Defense Research and Development Canada - Valcartier, 2459 Boulevard Pie-XI Nord, Quebec, QC. G3J 1X5 (Canada)

    2011-05-15

    Spray pyrolysis chemical vapor deposition (CVD) in the absence of hydrogen at low carrier gas flow rates has been used for the growth of carbon nanotubes (CNTs). A parametric study of the carbon nanotube growth has been conducted by optimizing various parameters such as temperature, injection speed, precursor volume, and catalyst concentration. Experimental observations and characterizations reveal that the growth rate, size and quality of the carbon nanotubes are significantly dependent on the reaction parameters. Scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy techniques were employed to characterize the morphology, structure and crystallinity of the carbon nanotubes. The synthesis process can be applied to both semiconducting silicon wafer and conducting substrates such as carbon microfibers and stainless steel plates. This approach promises great potential in building various nanodevices with different electron conducting requirements. In addition, the absence of hydrogen as a carrier gas and the relatively low synthesis temperature (typically 750 deg. C) qualify the spray pyrolysis CVD method as a safe and easy way to scale up the CNT growth, which is applicable in industrial production.

  16. Hydrogen-free spray pyrolysis chemical vapor deposition method for the carbon nanotube growth: Parametric studies

    International Nuclear Information System (INIS)

    Spray pyrolysis chemical vapor deposition (CVD) in the absence of hydrogen at low carrier gas flow rates has been used for the growth of carbon nanotubes (CNTs). A parametric study of the carbon nanotube growth has been conducted by optimizing various parameters such as temperature, injection speed, precursor volume, and catalyst concentration. Experimental observations and characterizations reveal that the growth rate, size and quality of the carbon nanotubes are significantly dependent on the reaction parameters. Scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy techniques were employed to characterize the morphology, structure and crystallinity of the carbon nanotubes. The synthesis process can be applied to both semiconducting silicon wafer and conducting substrates such as carbon microfibers and stainless steel plates. This approach promises great potential in building various nanodevices with different electron conducting requirements. In addition, the absence of hydrogen as a carrier gas and the relatively low synthesis temperature (typically 750 deg. C) qualify the spray pyrolysis CVD method as a safe and easy way to scale up the CNT growth, which is applicable in industrial production.

  17. Characterization of doped hydrogenated nanocrystalline silicon films prepared by plasma enhanced chemical vapour deposition

    Institute of Scientific and Technical Information of China (English)

    Wang Jin-Liang; Wu Er-Xing

    2007-01-01

    The B-and P-doped hydrogenated nanocrystalline silicon films (nc-Si:H) are prepared by plasma-enhanced chemical vapour deposition (PECVD) .The microstructures of doped nc-Si:H films are carefully and systematically char acterized by using high resolution electron microscopy (HREM) ,Raman scattering,x-ray diffraction (XRD) ,Auger electron spectroscopy (AES) ,and resonant nucleus reaction (RNR) .The results show that as the doping concentration of PH3 increases,the average grain size (d) tends to decrease and the crystalline volume percentage (Xc) increases simultaneously.For the B-doped samples,as the doping concentration of B2H6 increases,no obvious change in the value of d is observed,but the value of Xc is found to decrease.This is especially apparent in the case of heavy B2H6 doped samples,where the films change from nanocrystalline to amorphous.

  18. Design of an isopropanol–acetone–hydrogen chemical heat pump with exothermic reactors in series

    International Nuclear Information System (INIS)

    The isopropanol–acetone–hydrogen chemical heat pump system with a series of exothermic reactors in which the reaction temperatures decrease successively is proposed. This system shows the better energy performances as compared with the traditional system with a single exothermic reactor, especially when the higher upgraded temperature is need. At the same amounts of the heat released, the work input of the compressor and the heater are both reduced notably. The results indicate that the advantages of the IAH-CHP system with exothermic reactors in series are obvious. - Highlights: • We propose the IAH-CHP system with exothermic reactors in series. • The COP and exergy efficiency of the system increase by 7.6% and 10.3% respectively. • The work input of the system is reduced notably at the same quantity of heat released

  19. Realizing controllable graphene nucleation by regulating the competition of hydrogen and oxygen during chemical vapor deposition heating.

    Science.gov (United States)

    Zhang, Haoran; Zhang, Yaqian; Zhang, Yanhui; Chen, Zhiying; Sui, Yanping; Ge, Xiaoming; Deng, Rongxuan; Yu, Guanghui; Jin, Zhi; Liu, Xinyu

    2016-08-24

    Oxygen can passivate Cu surface active sites when graphene nucleates. Thus, the nucleation density is decreased. The CuO/Cu substrate was chosen for graphene domain synthesis in our study. The results indicate that the CuO/Cu substrate is beneficial for large-scale, single-crystal graphene domain synthesis. Graphene grown on the CuO/Cu substrate exhibits fewer nucleation sites than on Cu foils, suggesting that graphene follows an oxygen-dominating growth. Hydrogen treatment via a heating process could weaken the surface oxygen's role in limiting graphene nucleation under the competition of hydrogen and oxygen and could transfer the synthesis of graphene into a hydrogen-dominating growth. However, the competition only exists during the chemical vapor deposition heating process. For non-hydrogen heated samples, oxygen-dominating growth is experienced even though the samples are annealed in hydrogen for a long time after the heating process. With the temperature increases, the role of hydrogen gradually decreases. The balance of hydrogen and oxygen is adjusted by introducing hydrogen gas at a different heating temperatures. The oxygen concentration on the substrate surface is believed to determine the reactions mechanisms based on the secondary ion mass spectrometry test results. This study provides a new method for the controllable synthesis of graphene nucleation during a heating process. PMID:27506467

  20. Numerical modeling of gas mixing and bio-chemical transformations during underground hydrogen storage within the project H2STORE

    Science.gov (United States)

    Hagemann, B.; Feldmann, F.; Panfilov, M.; Ganzer, L.

    2015-12-01

    The change from fossil to renewable energy sources is demanding an increasing amount of storage capacities for electrical energy. A promising technological solution is the storage of hydrogen in the subsurface. Hydrogen can be produced by electrolysis using excessive electrical energy and subsequently converted back into electricity by fuel cells or engine generators. The development of this technology starts with adding small amounts of hydrogen to the high pressure natural gas grid and continues with the creation of pure underground hydrogen storages. The feasibility of hydrogen storage in depleted gas reservoirs is investigated in the lighthouse project H2STORE financed by the German Ministry for Education and Research. The joint research project has project members from the University of Jena, the Clausthal University of Technology, the GFZ Potsdam and the French National Center for Scientic Research in Nancy. The six sub projects are based on laboratory experiments, numerical simulations and analytical work which cover the investigation of mineralogical, geochemical, physio-chemical, sedimentological, microbiological and gas mixing processes in reservoir and cap rocks. The focus in this presentation is on the numerical modeling of underground hydrogen storage. A mathematical model was developed which describes the involved coupled hydrodynamic and microbiological effects. Thereby, the bio-chemical reaction rates depend on the kinetics of microbial growth which is induced by the injection of hydrogen. The model has been numerically implemented on the basis of the open source code DuMuX. A field case study based on a real German gas reservoir was performed to investigate the mixing of hydrogen with residual gases and to discover the consequences of bio-chemical reactions.

  1. Hydrogen

    Directory of Open Access Journals (Sweden)

    John O’M. Bockris

    2011-11-01

    Full Text Available The idea of a “Hydrogen Economy” is that carbon containing fuels should be replaced by hydrogen, thus eliminating air pollution and growth of CO2 in the atmosphere. However, storage of a gas, its transport and reconversion to electricity doubles the cost of H2 from the electrolyzer. Methanol made with CO2 from the atmosphere is a zero carbon fuel created from inexhaustible components from the atmosphere. Extensive work on the splitting of water by bacteria shows that if wastes are used as the origin of feed for certain bacteria, the cost for hydrogen becomes lower than any yet known. The first creation of hydrogen and electricity from light was carried out in 1976 by Ohashi et al. at Flinders University in Australia. Improvements in knowledge of the structure of the semiconductor-solution system used in a solar breakdown of water has led to the discovery of surface states which take part in giving rise to hydrogen (Khan. Photoelectrocatalysis made a ten times increase in the efficiency of the photo production of hydrogen from water. The use of two electrode cells; p and n semiconductors respectively, was first introduced by Uosaki in 1978. Most photoanodes decompose during the photoelectrolysis. To avoid this, it has been necessary to create a transparent shield between the semiconductor and its electronic properties and the solution. In this way, 8.5% at 25 °C and 9.5% at 50 °C has been reached in the photo dissociation of water (GaP and InAs by Kainthla and Barbara Zeleney in 1989. A large consortium has been funded by the US government at the California Institute of Technology under the direction of Nathan Lewis. The decomposition of water by light is the main aim of this group. Whether light will be the origin of the post fossil fuel supply of energy may be questionable, but the maximum program in this direction is likely to come from Cal. Tech.

  2. Production of hydrogen, liquid fuels, and chemicals from catalytic processing of bio-oils

    Science.gov (United States)

    Huber, George W; Vispute, Tushar P; Routray, Kamalakanta

    2014-06-03

    Disclosed herein is a method of generating hydrogen from a bio-oil, comprising hydrogenating a water-soluble fraction of the bio-oil with hydrogen in the presence of a hydrogenation catalyst, and reforming the water-soluble fraction by aqueous-phase reforming in the presence of a reforming catalyst, wherein hydrogen is generated by the reforming, and the amount of hydrogen generated is greater than that consumed by the hydrogenating. The method can further comprise hydrocracking or hydrotreating a lignin fraction of the bio-oil with hydrogen in the presence of a hydrocracking catalyst wherein the lignin fraction of bio-oil is obtained as a water-insoluble fraction from aqueous extraction of bio-oil. The hydrogen used in the hydrogenating and in the hydrocracking or hydrotreating can be generated by reforming the water-soluble fraction of bio-oil.

  3. Chemical kinetic analysis of hydrogen-air ignition and reaction times

    Science.gov (United States)

    Rogers, R. C.; Schexnayder, C. J., Jr.

    1981-01-01

    An anaytical study of hydrogen air kinetics was performed. Calculations were made over a range of pressure from 0.2 to 4.0 atm, temperatures from 850 to 2000 K, and mixture equivalence ratios from 0.2 to 2.0. The finite rate chemistry model included 60 reactions in 20 species of the H2-O2-N2 system. The calculations also included an assessment of how small amounts of the chemicals H2O, NOx, H2O2, and O3 in the initial mixture affect ignition and reaction times, and how the variation of the third body efficiency of H2O relative of N2 in certain key reactions may affect reaction time. The results indicate that for mixture equivalence ratios between 0.5 and 1.7, ignition times are nearly constant; however, the presence of H2O and NO can have significant effects on ignition times, depending on the mixture temperature. Reaction time is dominantly influenced by pressure but is nearly independent of initial temperature, equivalence ratio, and the addition of chemicals. Effects of kinetics on reaction at supersonic combustor conditions are discussed.

  4. Chemical aspects of hydrogen ingress in zirconium and zircaloy pressure tubes: ageing management of Indian PHWR coolant channels - determination of hydrogen and deuterium

    International Nuclear Information System (INIS)

    Pressurized heavy water reactors (PHWRs) use zirconium and zirconium based alloys as clad and coolant tubes since its beginning. The first ever zircaloy-2 pressure tube failure occurred in 1983 at Ontario Hydro's Pickering Unit 2 in Canada which necessitated a thorough examination of causes of such failure. The failure was attributed to massive hydriding at the failed spot of pressure tube. Continuous usage of zirconium alloys could result in their hydrogen and deuterium pick-up leading to hydrogen/ deuterium embrittlement. The life of the zircaloy coolant channels is dictated by hydrogen/deuterium content and hence ageing management of the pressure tubes is essential for ensuring their trouble-free usage. It is desirable to have a sound knowledge on the chemical aspects of zirconium and zirconium based alloys metallurgy, the mechanistic principles of hydrogen ingress into the pressure tubes during in reactor service, and identifying suitable analytical methodologies for precise and accurate determination of hydrogen in wafer thin sliver samples carved out from insides of pressure tubes without causing any structural damage so that it can continue to remain in service. This is desirable so that the ageing management does not result in cost-escalation. This report is divided in to three main parts. The first part deals with the chemical aspects of zirconium and zirconium based alloy metallurgy, the mechanism of hydrogen pick-up and hydride formation in zirconium matrix. The second part describes various methodologies and their limitations, available for hydrogen/deuterium determination. The third part deals in detail, about the extensive investigations carried out at Radioanalytical Chemistry Division (RACD) in Radiochemistry and Isotope Group for establishing an indigenously developed hot vacuum extraction system in combination with quadrupole mass spectrometry for precise determination of hydrogen and deuterium in wafer thin sliver sample of zircaloy. The

  5. Plasma-chemical treatment of hydrogen sulfide in natural gas processing. Final report, May 1991--December 1992

    Energy Technology Data Exchange (ETDEWEB)

    Harkness, J.B.L.; Doctor, R.D. [Argonne National Lab., IL (United States)

    1993-05-01

    A new process for the treatment of hydrogen sulfide waste that uses microwave plasma-chemical technology has been under development in Russia and the United States. Whereas the present waste-treatment technology, at best, only recovers sulfur, this novel process recovers both hydrogen and sulfur by dissociating hydrogen sulfide in a plasma by means of a microwave or radio-frequency reactor. A research project has been undertaken to determine the suitability of the plasma process in natural gas processing applications. The experiments tested acid-gas compositions with 30--65% carbon dioxide, 0--7% water, and 0--0.2% of a standard mixture of pipeline gas. The balance gas in all cases was hydrogen sulfide. The reactor pressure for the experiments was 50 torr, and the microwave power was 1.0 kW. Conversions of hydrogen sulfide ranged from 80 to 100%, while 35--50% of the carbon dioxide was converted to carbon monoxide. This conversion of carbon dioxide resulted in a loss of hydrogen production and an energy loss from a hydrogen sulfide waste-treatment perspective. Tests of a direct natural gas treatment concept showed that hydrocarbon losses were unacceptably high; consequently, the concept would not be economically viable.

  6. Chemical equilibrium of hydrogen and aqueous solutions of 1 : 1 bicarbonate and formate salts with a common cation

    NARCIS (Netherlands)

    Engel, D.C.; Versteeg, G.F.; Swaaij, W.P.M. van

    1997-01-01

    The chemical equilibrium of hydrogen and aqueous solutions of 1:1 bicarbonate and formate salts with a common cation has been investigated in an intensively stirred batch reactor: MHCO3(aq) + H2(aq) ↔ MOOCH(aq) + H2O(l) This was accomplished for the sodium (M = Na), potassium (M = K) and ammonium (M

  7. Hydrogen system (hydrogen fuels feasibility)

    International Nuclear Information System (INIS)

    This feasibility study on the production and use of hydrogen fuels for industry and domestic purposes includes the following aspects: physical and chemical properties of hydrogen; production methods steam reforming of natural gas, hydrolysis of water; liquid and gaseous hydrogen transportation and storage (hydrogen-hydride technology); environmental impacts, safety and economics of hydrogen fuel cells for power generation and hydrogen automotive fuels; relevant international research programs

  8. Energy Efficient Catalytic Activation of Hydrogen peroxide for Green Chemical Processes: Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Collins, Terrence J.; Horwitz, Colin

    2004-11-12

    A new, highly energy efficient approach for using catalytic oxidation chemistry in multiple fields of technology has been pursued. The new catalysts, called TAML® activators, catalyze the reactions of hydrogen peroxide and other oxidants for the exceptionally rapid decontamination of noninfectious simulants (B. atrophaeus) of anthrax spores, for the energy efficient decontamination of thiophosphate pesticides, for the facile, low temperature removal of color and organochlorines from pulp and paper mill effluent, for the bleaching of dyes from textile mill effluents, and for the removal of recalcitrant dibenzothiophene compounds from diesel and gasoline fuels. Highlights include the following: 1) A 7-log kill of Bacillus atrophaeus spores has been achieved unambiguously in water under ambient conditions within 15 minutes. 2) The rapid total degradation under ambient conditions of four thiophosphate pesticides and phosphonate degradation intermediates has been achieved on treatment with TAML/peroxide, opening up potential applications of the decontamination system for phosphonate structured chemical warfare agents, for inexpensive, easy to perform degradation of stored and aged pesticide stocks (especially in Africa and Asia), for remediation of polluted sites and water bodies, and for the destruction of chemical warfare agent stockpiles. 3) A mill trial conducted in a Pennsylvanian bleached kraft pulp mill has established that TAML catalyst injected into an alkaline peroxide bleach tower can significantly lower color from the effluent stream promising a new, more cost effective, energy-saving approach for color remediation adding further evidence of the value and diverse engineering capacity of the approach to other field trials conducted on effluent streams as they exit the bleach plant. 4) Dibenzothiophenes (DBTs), including 4,6-dimethyldibenzothiophene, the most recalcitrant sulfur compounds in diesel and gasoline, can be completely removed from model gasoline

  9. Combustion of hydrogen-air jets in local chemical equilibrium: A guide to the CHARNAL computer program

    Science.gov (United States)

    Spalding, D. B.; Launder, B. E.; Morse, A. P.; Maples, G.

    1974-01-01

    A guide to a computer program, written in FORTRAN 4, for predicting the flow properties of turbulent mixing with combustion of a circular jet of hydrogen into a co-flowing stream of air is presented. The program, which is based upon the Imperial College group's PASSA series, solves differential equations for diffusion and dissipation of turbulent kinetic energy and also of the R.M.S. fluctuation of hydrogen concentration. The effective turbulent viscosity for use in the shear stress equation is computed. Chemical equilibrium is assumed throughout the flow.

  10. Midplane Pressure and the Abundance of Molecular Hydrogen in Galaxies: Non-Equilibrium Chemical Models

    CERN Document Server

    Mac Low, Mordecai-Mark

    2010-01-01

    Observations of spiral galaxies show a strong linear correlation between midplane pressure and the ratio of molecular to atomic hydrogen surface density R_mol. It has been suggested that this occurs because of the equilibrium balance between radiative dissociation and H_2 formation on dust grains. We use a three-dimensional, numerical model of magnetized turbulence including a simplified chemical network and treatment of the propagation of dissociating radiation to follow the formation of H_2 from cold atomic gas. This model allows us to examine the origin of the observed correlation. We find that the formation time scale for H_2 is sufficiently long that equilibrium is not reached within the 20-30 Myr lifetimes of molecular clouds. Equilibrium models of molecular clouds do not predict the time-dependent molecular fractions we find, so the observed correlation seems unlikely to be explained by them. Our simulations do show that a simple, time-dependent model of H_2 formation can reproduce the gross behavior, ...

  11. Inhibition of hydrogen sulfide generation from disposed gypsum drywall using chemical inhibitors

    International Nuclear Information System (INIS)

    Disposal of gypsum drywall in landfills has been demonstrated to elevate hydrogen sulfide (H2S) concentrations in landfill gas, a problem with respect to odor, worker safety, and deleterious effect on gas-to-energy systems. Since H2S production in landfills results from biological activity, the concept of inhibiting H2S production through the application of chemical agents to drywall during disposal was studied. Three possible inhibition agents - sodium molybdate (Na2MoO4), ferric chloride (FeCl3), and hydrated lime (Ca(OH)2) - were evaluated using flask and column experiments. All three agents inhibited H2S generation, with Na2MoO4 reducing H2S generation by interrupting the biological sulfate reduction process and Ca(OH)2 providing an unfavorable pH for biological growth. Although FeCl3 was intended to provide an electron acceptor for a competing group of bacteria, the mechanism found responsible for inhibiting H2S production in the column experiment was a reduction in pH. Application of both Na2MoO4 and FeCl3 inhibited H2S generation over a long period (over 180 days), but the impact of Ca(OH)2 decreased with time as the alkalinity it contributed was neutralized by the generated H2S. Practical application and potential environmental implications need additional exploration.

  12. Characterizing the chemical pathways for water formation -- A deep search for hydrogen peroxide

    CERN Document Server

    Parise, B; Menten, K

    2014-01-01

    In 2011, hydrogen peroxide (HOOH) was observed for the first time outside the solar system (Bergman et al., A&A, 2011, 531, L8). This detection appeared a posteriori quite natural, as HOOH is an intermediate product in the formation of water on the surface of dust grains. Following up on this detection, we present a search for HOOH in a diverse sample of sources in different environments, including low-mass protostars and regions with very high column densities, such as Infrared Dark Clouds (IRDCs). We do not detect the molecule in any other source than Oph A, and derive 3$\\sigma$ upper limits for the abundance of HOOH relative to H$_2$ lower than in Oph A for most sources. This result sheds a different light on our understanding of the detection of HOOH in Oph A, and shifts the puzzle to why this source seems to be special. Therefore we rediscuss the detection of HOOH in Oph A, as well as the implications of the low abundance of HOOH, and its similarity with the case of O$_2$. Our chemical models show th...

  13. Inhibition of hydrogen sulfide generation from disposed gypsum drywall using chemical inhibitors.

    Science.gov (United States)

    Xu, Qiyong; Townsend, Timothy; Bitton, Gabriel

    2011-07-15

    Disposal of gypsum drywall in landfills has been demonstrated to elevate hydrogen sulfide (H(2)S) concentrations in landfill gas, a problem with respect to odor, worker safety, and deleterious effect on gas-to-energy systems. Since H(2)S production in landfills results from biological activity, the concept of inhibiting H(2)S production through the application of chemical agents to drywall during disposal was studied. Three possible inhibition agents - sodium molybdate (Na(2)MoO(4)), ferric chloride (FeCl(3)), and hydrated lime (Ca(OH)(2)) - were evaluated using flask and column experiments. All three agents inhibited H(2)S generation, with Na(2)MoO(4) reducing H(2)S generation by interrupting the biological sulfate reduction process and Ca(OH)(2) providing an unfavorable pH for biological growth. Although FeCl(3) was intended to provide an electron acceptor for a competing group of bacteria, the mechanism found responsible for inhibiting H(2)S production in the column experiment was a reduction in pH. Application of both Na(2)MoO(4) and FeCl(3) inhibited H(2)S generation over a long period (over 180 days), but the impact of Ca(OH)(2) decreased with time as the alkalinity it contributed was neutralized by the generated H(2)S. Practical application and potential environmental implications need additional exploration. PMID:21592650

  14. Research on the Interaction of Hydrogen-Bond Acidic Polymer Sensitive Sensor Materials with Chemical Warfare Agents Simulants by Inverse Gas Chromatography

    OpenAIRE

    Liu Yang; Qiang Han; Shuya Cao; Feng Huang; Molin Qin; Chenghai Guo; Mingyu Ding

    2015-01-01

    Hydrogen-bond acidic polymers are important high affinity materials sensitive to organophosphates in the chemical warfare agent sensor detection process. Interactions between the sensor sensitive materials and chemical warfare agent simulants were studied by inverse gas chromatography. Hydrogen bonded acidic polymers, i.e., BSP3, were prepared for micro-packed columns to examine the interaction. DMMP (a nerve gas simulant) and 2-CEES (a blister agent simulant) were used as probes. Chemical an...

  15. Application of Ozone and Oxygen to Reduce Chemical Oxygen Demand and Hydrogen Sulfide from a Recovered Paper Processing Plant

    Directory of Open Access Journals (Sweden)

    Patricia A. Terry

    2010-01-01

    Full Text Available A pilot study was performed at the Fox River Fiber recovered paper processing company in DePere, Wisconsin, to determine the extent to which injection of oxygen and ozone could reduce the high chemical oxygen demand, COD, in the effluent and the effectiveness of the ozone/oxygen stream in suppressing production of hydrogen sulfide gas in downstream sewage lines. Adaptive Ozone Solutions, LLC, supplied the oxygen/ozone generation and injection system. Samples were analyzed both before and after oxygen/ozone injection. Hydrogen sulfide gas was continuously monitored at sewer stations downstream of Fox River Fiber. Results showed that with a very short contact time, effluent COD was reduced by over 15%. A simple kinetic model predicts that a contact time of fewer than 30 minutes could reduce COD by as much as 60%. In addition, downstream hydrogen sulfide gas production in the sewage mains was also better controlled, such that costly Bioxide applications could be reduced.

  16. Immobilization of redox mediators on functionalized carbon nanotube: A material for chemical sensor fabrication and amperometric determination of hydrogen peroxide

    Indian Academy of Sciences (India)

    D R Shobha Jeykumari; S Senthil Kumar; S Sriman Narayanan

    2005-10-01

    Chemical functionalization of single-walled carbon nanotubes with redox mediators, namely, toluidine blue and thionin have been carried out and the performance of graphite electrode modified with functionalized carbon nanotubes is described. Mechanical immobilization of functionalized single-walled nanotube (SWNT) on graphite electrode was achieved by gently rubbing the electrode surface on carbon nanotubes supported on a glass slide. The electrochemical behaviour of the modified electrodes was investigated by cyclic voltammetry. The SWNT-modified electrodes showed excellent electrocatalytic effect for the reduction of hydrogen peroxide. A decrease in overvoltage was observed as well as an enhanced peak current compared to a bare graphite electrode for the reduction of hydrogen peroxide. The catalytic current was found to be directly proportional to the amount of hydrogen peroxide taken.

  17. Prospects for pipeline delivery of hydrogen as a fuel and as a chemical feedstock

    Science.gov (United States)

    Gregory, D. P.; Biederman, N. P.; Darrow, K. G., Jr.; Konopka, A. J.; Wurm, J.

    1976-01-01

    The possibility of using hydrogen for storing and carrying energy obtained from nonfossil sources such as nuclear and solar energy is examined. According to the method proposed, these nonfossil raw energy sources will be used to obtain hydrogen from water by three basically distinct routes: (1) electrical generation followed by electrolysis; (2) thermochemical decomposition; and (3) direct neutron or ultraviolet irradiation of hydrogen bearing molecules. The hydrogen obtained will be transmitted in long-distance pipelines, and distributed to all energy-consuming sectors. As a fuel gas, hydrogen has many qualities similar to natural gas and with only minor modifications, it can be transmitted and distributed in the same equipment, and can be burned in the same appliances as natural gas. Hydrogen can also be used as a clean fuel (water is the only combustion product) for automobiles, fleet vehicles, and aircraft.

  18. New horizons in chemical propulsion. [processes using free radicals, atomic hydrogen, excited species, etc

    Science.gov (United States)

    Cohen, W.

    1973-01-01

    After a review of the work of the late-Fifties on free radicals for propulsion, it is concluded that atomic hydrogen would provide a potentially large increase in specific impulse. Work conducted to find an approach for isolating atomic hydrogen is considered. Other possibilities for obtaining propellants of greatly increased capability might be connected with the technology for the generation of activated states of gases, metallic hydrogen, fuels obtained from other planets, and laser transfer of energy.

  19. Thermodynamic Feasibility of Hydrogen-Rich Gas Production Supported by Iron Based Chemical Looping Process

    OpenAIRE

    Słowiński, Grzegorz; Smoliński, Adam

    2016-01-01

    The continuously increasing oil prices as well as stronger environmental regulations regarding greenhouse emissions made the greatest economic powers search a new, price competitive, and environment friendly energy carrier, such as hydrogen. The world research activities in these terms focus on the development of integrated hydrogen and power generating technologies, particularly technologies of hydrogen production from various carbonaceous resources, like methane, coal, biomass, or waste, of...

  20. Hot bubbles of planetary nebulae with hydrogen-deficient winds I. Heat conduction in a chemically stratified plasma

    CERN Document Server

    Sandin, Christer; Schönberner, Detlef; Rühling, Ute

    2016-01-01

    Heat conduction has been found a plausible solution to explain discrepancies between expected and measured temperatures in hot bubbles of planetary nebulae (PNe). While the heat conduction process depends on the chemical composition, to date it has been exclusively studied for pure hydrogen plasmas in PNe. A smaller population of PNe show hydrogen-deficient and helium- and carbon-enriched surfaces surrounded by bubbles of the same composition; considerable differences are expected in physical properties of these objects in comparison to the pure hydrogen case. The aim of this study is to explore how a chemistry-dependent formulation of the heat conduction affects physical properties and how it affects the X-ray emission from PN bubbles of hydrogen-deficient stars. We extend the description of heat conduction in our radiation hydrodynamics code to work with any chemical composition. We then compare the bubble-formation process with a representative PN model using both the new and the old descriptions. We also ...

  1. Purification of hydrogen under a free or combined form in a gaseous mixture, by chemical reactions with uranium

    International Nuclear Information System (INIS)

    Within the framework of the european fusion program, we are dealing with the purification of hydrogen (tritium) under a free or combined form, from a H2, N2, NH3, CH4, O2, gaseous mixture. The process consists in cracking the hydrogenated molecules and absorbing the impurities by chemical reactions with uranium, without holding back hydrogen. In the temperature range: 950 K < T < 1200 K hydrides are indeed fully decomposed for hydrogen partial pressures lower than ten atmospheres while uranium oxides, nitrides and carbides formation reactions are promoted. The experiments are carried out with massive uranium heated at 973 K in a closed reactor. They confirm that such a process may satisfy our goals, but they point out the importance of interactions occurring between the gaseous and solids systems and interfere with the conversion rates. Gaseous pressure decreases with time according to two successive phases: the first one is governed by a surface kinetic law, while after a short transition time, gas diffusion in the solid products arises and becomes the limiting step of the reactions. Experimental results with pure gases and mixtures, prove that solid products have different structures. An illustrative example is given by nitrogen and methane reactions with uranium: the solid layers are compactely formed with each pure gas and they slow down the chemical kinetic rates; on the contrary the chemical kinetic rates of the mixed gases reactions are clearly increased and the diffusional rates are postponed. Then, the compacity of the solid products merely depends on the operating conditions and the influence of the reactional surface state on the chemical kinetic rates is here pointed out

  2. Flexible Electronics: High Pressure Chemical Vapor Deposition of Hydrogenated Amorphous Silicon Films and Solar Cells (Adv. Mater. 28/2016).

    Science.gov (United States)

    He, Rongrui; Day, Todd D; Sparks, Justin R; Sullivan, Nichole F; Badding, John V

    2016-07-01

    On page 5939, J. V. Badding and co-workers describe the unrolling of a flexible hydrogenated amorphous silicon solar cell, deposited by high-pressure chemical vapor deposition. The high-pressure deposition process is represented by the molecules of silane infiltrating the small voids between the rolled up substrate, facilitating plasma-free deposition over a very large area. The high-pressure approach is expected to also find application for 3D nanoarchitectures. PMID:27442970

  3. Influence of chemical activation of a 35% hydrogen peroxide bleaching gel on its penetration and efficacy--in vitro study

    OpenAIRE

    Torres, C R G; Wiegand, A.; Sener, B.; Attin, T.

    2010-01-01

    OBJECTIVES: The aim of this study was to evaluate the effects of chemical activation of hydrogen peroxide (HP) gel on colour changes and penetration through the tooth structure. METHODS: One hundred and four bovine incisors were used. One dentine (CD) disc and one enamel-dentine (ED) disc were prepared from each tooth. They were positioned over artificial pulpal chambers and the bleaching was performed with an experimental 35% HP gel. Two control and six experimental groups were prepared. In ...

  4. Quantum chemical approach for condensed-phase thermochemistry (III): Accurate evaluation of proton hydration energy and standard hydrogen electrode potential

    Science.gov (United States)

    Ishikawa, Atsushi; Nakai, Hiromi

    2016-04-01

    Gibbs free energy of hydration of a proton and standard hydrogen electrode potential were evaluated using high-level quantum chemical calculations. The solvent effect was included using the cluster-continuum model, which treated short-range effects by quantum chemical calculations of proton-water complexes, and the long-range effects by a conductor-like polarizable continuum model. The harmonic solvation model (HSM) was employed to estimate enthalpy and entropy contributions due to nuclear motions of the clusters by including the cavity-cluster interactions. Compared to the commonly used ideal gas model, HSM treatment significantly improved the contribution of entropy, showing a systematic convergence toward the experimental data.

  5. The behaviour of chemically altered coals in ZnCl{sub 2}-catalysed reaction with hydrogen and methanol

    Energy Technology Data Exchange (ETDEWEB)

    Kuznetsov, P.N.; Bimer, J.; Salbut, P.D.; Gruber, R.; Djega-Mariadassou, G.; Brodzki, D.; Korniyets, E.; Kuznetsova, L.; Krzton, A. [Institute of Chemistry and Chemico-Metallurgical Processes, Krasnoyarsk (Russian Federation)

    1996-08-01

    A series of chemically altered coals was investigated in the reaction with methanol and hydrogen in the presence of ZnCl{sub 2} as a catalyst. Significant beneficial effects were observed when high-rank coals were altered by reductive and radioactively methylating pretreatments. The behaviour of altered low-rank brown and subbituminous coals was affected by both the mode of chemical pretreatment and the reaction conditions. The benefit can be explained by partial depolymerization of the coal matter through the disruption of cross-links and the passivation of hydroxyl groups by methylation. 33 refs., 7 figs., 3 tabs.

  6. The impact of soil uptake on the global distribution of molecular hydrogen: chemical transport model simulation

    Directory of Open Access Journals (Sweden)

    H. Yashiro

    2011-07-01

    Full Text Available The global tropospheric distribution of molecular hydrogen (H2 and its uptake by the soil are simulated using a model called CHemical AGCM (atmospheric general circulation model for the Study of the Environment and Radiative forcing (CHASER, which incorporates a two-layered soil diffusion/uptake process component. The simulated distribution of deposition velocity over land is influenced by regional climate, and has a global average of 3.3×10−2 cm s−1. In the region north of 30° N, the amount of soil uptake shows a large seasonal variation corresponding to change in biological activity due to soil temperature and change in diffusion suppression by snow cover. In the temperate and humid regions in the mid- to low- latitudes, the uptake is mostly influenced by the soil air ratio, which controls the gas diffusivity in the soil. In the semi-arid regions, water stress and high temperatures contribute to the reduction of biological activity, as well as to the seasonal variation in the deposition velocity. A comparison with the observations shows that the model reproduces both the distribution and seasonal variation of H2 relatively well. The global burden and tropospheric lifetime of H2 are 150 Tg and 2.0 yr, respectively. The seasonal variation in H2 mixing ratios at the northern high latitudes is mainly controlled by a large seasonal change in the soil uptake. In the Southern Hemisphere, seasonal change in net chemical production and inter-hemispheric transport are the dominant causes of the seasonal cycle, while large biomass burning contributes significantly to the seasonal variation in the tropics and subtropics. Both observations and the model show large inter-annual variations, especially for the period 1997–1998, associated with large biomass burning in the tropics and at Northern Hemisphere high latitudes. The soil uptake shows relatively small inter-annual variability

  7. The impact of soil uptake on the global distribution of molecular hydrogen: chemical transport model simulation

    Directory of Open Access Journals (Sweden)

    H. Yashiro

    2011-02-01

    Full Text Available The molecular hydrogen (H2 in the troposphere is highly influenced by the strength of H2 uptake by the terrestrial soil surface. The global distribution of H2 and its uptake by the soil are simulated by using a model called CHemical AGCM for Study of Environment and Radiative forcing (CHASER, which incorporates a 2-layered soil diffusion/uptake process component. The simulated distribution of deposition velocity over land reflects regional climate and has a global average of 3.3 × 10−2 cm s−1. In the region north of 30° N, the amount of soil uptake increases, particularly in the summer. However, the increase in the uptake becomes smaller in the winter season due to snow cover and a reduction in the biological activity at low temperatures. In the temperate and humid regions in the mid- and low-latitudes, the uptake is mostly influenced by the soil air ratio, which controls the gas diffusivity in the soil. In the semi-arid region, water stress and high temperature contribute to the reduction of biological activity, as well as to the seasonal variation in the deposition velocity. The comparison with the observations shows that the model reproduces both the distribution and seasonal variation of H2 relatively well. The global burden and tropospheric lifetime are 150 Tg and 2.0 yr, respectively. The seasonal variation of H2 in the northern high latitude is mainly controlled by the large seasonal change in soil uptake. In the Southern Hemisphere, the seasonal change in the net chemical production and inter-hemispheric transport are the dominant cause of the seasonal cycle. Large biomass burning impacts the magnitude of seasonal variation mainly in the tropics and subtropics. Both observation and model show large inter-annual variation, especially for the period 1997–1998, associated with the large biomass burning in tropics and northern high-latitudes. The soil uptake

  8. Enhanced thermophilic fermentative hydrogen production from cassava stillage by chemical pretreatments

    DEFF Research Database (Denmark)

    Wang, Wen; Luo, Gang; Xie, Li;

    2013-01-01

    Acid and alkaline pretreatments for enhanced hydrogen production from cassava stillage were investigated in the present study. The result showed that acid pretreatment was suitable for enhancement of soluble carbohydrate while alkaline pretreatment stimulated more soluble total organic carbon...... production from cassava stillage. Acid pretreatment thereby has higher capacity to promote hydrogen production compared with alkaline pretreatment. Effects of pretreatment temperature, time and acid concentration on hydrogen production were also revealed by response surface methodology. The results showed...... production of 434 mL, 67% higher than raw cassava stillage....

  9. Proceedings of the DOE Chemical Energy Storage and Hydrogen Energy Systems Contracts Review

    Science.gov (United States)

    Kelley, J. H.

    1978-01-01

    The background and objectives of thirty-nine hydrogen-related tasks were discussed, the status of the studies or technical effort is shown, and state projected solutions for resolving the identified problems are projected.

  10. Prospects for pipeline delivery of hydrogen as a fuel and as a chemical feedstock

    Energy Technology Data Exchange (ETDEWEB)

    Gregory, D.P.; Biederman, N.P.; Darrow, K.G. Jr.; Konopka, A.J.; Wurm, J.

    1976-01-01

    The prospects for hydrogen pipelining over long distances are very real, as is the need to develop this capability. The technical problems involved do not appear to be too severe, but there are still some unknown quantities that require research and development, not the least of which is concerned with possible hydrogen embrittlement. The gas industry has many opportunities to become involved with future energy technology by means of its present capability to transmit gaseous energy over long distances. The initial concept of the ''hydrogen economy'' was a somewhat idealistic approach to solving the national energy problem with a completely new energy distribution system. After a few years of study of this concept, some rather more realistic and somewhat more limited options are emerging that will involve the pipelining of hydrogen and should involve the gas industry.

  11. Extend of hydrogen coverage of Si(001) under chemical vapor deposition conditions from ab initio approaches

    CERN Document Server

    Rosenow, Phil

    2016-01-01

    The extent of hydrogen coverage of the Si(001)c(4x2) surface in the presence of hydrogen gas has been studied with dispersion corrected density functional theory. Electronic energy contributions are well described using a hybrid functional. The temperature dependence of the coverage in thermodynamic equilibrium was studied computing the phonon spectrum in a supercell approach. As an approximation to these demanding computations, an interpolated phonon approach was found to give comparable accuracy. The simpler ab initio thermodynamic approach is not accurate enough for the system studied, even if corrections by the Einstein model for surface vibrations are considered. The on-set of H2 desorption from the fully hydrogenated surface is predicted to occur at temperatures around 750 K. Strong changes in hydrogen coverage are found between 1000 and 1200 K in good agreement with previous reflectance anisotropy spectroscopy experiments. These findings allow a rational choice for the surface state in the computationa...

  12. Modelling a DR shaft operated with pure hydrogen using a physical-chemical and CFD approach

    OpenAIRE

    Ranzani Da Costa, Andrea; Wagner, D.; Patisson, F.; Ablitzer, D.

    2009-01-01

    International audience The hydrogen-based route could be a valuable way to produce steel considering its low carbon dioxide emissions. In ULCOS, it is regarded as a long-term option, largely dependent on the emergence of a hydrogen economy. To anticipate its possible development, it was decided to check the feasibility of using 100% H2 in a Direct Reduction shaft furnace and to determine the best operating conditions, through appropriate experimental and modelling work. We developed from s...

  13. High precision quantum-chemical treatment of adsorption: Benchmarking physisorption of molecular hydrogen on graphane

    Energy Technology Data Exchange (ETDEWEB)

    Usvyat, Denis, E-mail: denis.usvyat@chemie.uni-regensburg.de [Institute for Physical and Theoretical Chemistry, Universität Regensburg, Universitätsstrasse 31, D-93040 Regensburg (Germany)

    2015-09-14

    A multilevel hierarchical ab initio protocol for calculating adsorption on non-conducting surfaces is presented. It employs fully periodic treatment, which reaches local Møller-Plesset perturbation theory of second order (MP2) with correction for the basis set incompleteness via the local F12 technique. Post-MP2 corrections are calculated using finite clusters. That includes the coupled cluster treatment in the local and canonical frameworks (up to perturbative quadruples) and correlated core (with MP2). Using this protocol, the potential surface of hydrogen molecules adsorbed on graphane was computed. According to the calculations, hydrogen molecules are adsorbed on graphane in a perpendicular to the surface orientation with the minimum of the potential surface of around −3.6 kJ/mol located at the distance of 3.85 Å between the bond center of the hydrogen molecule and the mid-plane of graphane. The adsorption sites along the path from the downward-pointing carbon to the ring center of the graphane are energetically virtually equally preferable, which can enable nearly free translations of hydrogen molecules along these paths. Consequently, the hydrogen molecules on graphane most likely form a non-commensurate monolayer. The analysis of the remaining errors reveals a very high accuracy of the computed potential surface with an error bar of a few tenths of a kJ/mol. The obtained results are a high-precision benchmark for further theoretical and experimental studies of hydrogen molecules interacting with graphane.

  14. High precision quantum-chemical treatment of adsorption: Benchmarking physisorption of molecular hydrogen on graphane

    Science.gov (United States)

    Usvyat, Denis

    2015-09-01

    A multilevel hierarchical ab initio protocol for calculating adsorption on non-conducting surfaces is presented. It employs fully periodic treatment, which reaches local Møller-Plesset perturbation theory of second order (MP2) with correction for the basis set incompleteness via the local F12 technique. Post-MP2 corrections are calculated using finite clusters. That includes the coupled cluster treatment in the local and canonical frameworks (up to perturbative quadruples) and correlated core (with MP2). Using this protocol, the potential surface of hydrogen molecules adsorbed on graphane was computed. According to the calculations, hydrogen molecules are adsorbed on graphane in a perpendicular to the surface orientation with the minimum of the potential surface of around -3.6 kJ/mol located at the distance of 3.85 Å between the bond center of the hydrogen molecule and the mid-plane of graphane. The adsorption sites along the path from the downward-pointing carbon to the ring center of the graphane are energetically virtually equally preferable, which can enable nearly free translations of hydrogen molecules along these paths. Consequently, the hydrogen molecules on graphane most likely form a non-commensurate monolayer. The analysis of the remaining errors reveals a very high accuracy of the computed potential surface with an error bar of a few tenths of a kJ/mol. The obtained results are a high-precision benchmark for further theoretical and experimental studies of hydrogen molecules interacting with graphane.

  15. Analysis of the number of hydrogen bond groups of a multiwalled carbon nanotube probe tip for chemical force microscopy

    International Nuclear Information System (INIS)

    In this paper, we describe a statistical method of quantification of the number of functional groups at the contact area of a probe tip for atomic force microscopy from the result of repetitive pull-off force measurements. We have investigated laboratory-made carbon nanotube (CNT) probe tips to apply them for chemical force microscopy because limited number of functional groups at the tip-end is expected. Using a CNT tip, we conducted repetitive pull-off force measurements against a self-assembled monolayer terminated with carboxyl group and analyzed them in terms of the number of hydrogen bond groups at the CNT tip. The elementary hydrogen bond rupture force quantum in n-decane medium was estimated to be 84.2 ± 0.5 pN in the present system. Thus it was revealed that only a couple of hydrogen bond groups of the CNT tip were participating in hydrogen bonding with the sample on an average in this experimental system.

  16. Influence of hydrogen on chemical vapour synthesis of different carbon nanostructures using propane as precursor and nickel as catalyst

    Indian Academy of Sciences (India)

    R K Sahoo; H Mamgain; C Jacob

    2014-10-01

    The role of hydrogen in the catalytic chemical vapour deposition of carbon nanotubes using sputtered nickel thin film as a catalyst is explained in this work. The growth of different carbon nanostructures with the variation in the precursor gas content was studied by keeping all other process parameters constant and using sputtered Ni thin film as a catalyst. The catalyst granule size, its external morphology and the resulting products were analysed. Carbon nanotubes (CNTs), carbon nanofibres (CNFs) and carbon nanoribbons (CNRs) were observed under different growth conditions. The different conditions of growth leading to form tubes, fibres or ribbons were analysed by varying the flow ratio of propane and hydrogen gas during the high temperature growth. Scanning and transmission electron microscopies confirmed the above structures under different growth conditions. The role of hydrogen on the surface passivation behaviour of the Ni catalyst and its correlative effect on the growth of carbon nanostructures is analysed. This direct approach can, in principle, be used to synthesize different types of carbon nanostructures by tailoring the hydrogen concentration.

  17. Selective deposition of a crystalline Si film by a chemical sputtering process in a high pressure hydrogen plasma

    International Nuclear Information System (INIS)

    The selective deposition of Si films was demonstrated using a chemical sputtering process induced by a high pressure hydrogen plasma at 52.6 kPa (400 Torr). In this chemical sputtering process, the initial deposition rate (Rd) is dependent upon the substrate type. At the initial stage of Si film formation, Rd on glass substrates increased with elapsed time and reached to a constant value. In contrast, Rd on Si substrates remained constant during the deposition. The selective deposition of Si films can be achieved by adjusting the substrate temperature (Tsub) and hydrogen concentration (CH2) in the process atmosphere. For any given deposition time, it was found that an optimum CH2 exists for a given Tsub to realize the selective deposition of a Si film, and the optimum Tsub value tends to increase with decreasing CH2. According to electron diffraction patterns obtained from the samples, the selectively prepared Si films showed epitaxial-like growth, although the Si films contained many defects. It was revealed by Raman scattering spectroscopy that some of the defects in the Si films were platelet defects induced by excess hydrogen incorporated during Si film formation. Raman spectrum also suggested that Si related radicals (SiH2, SiH, Si) with high reactivity contribute to the Si film formation. Simple model was derived as the guideline for achieving the selective growth

  18. Mobility and chemical bond of hydrogen in titanium and palladium hydrides

    International Nuclear Information System (INIS)

    The probabilities for π- meson capture by hydrogen are measured at 25, 155 and 200 deg C in TiHsub(1.65) hydride and at 25, -120 and -196 deg C in PdHsub(0.67) hydride. An analysis of the results obtained shows that within the accuracy of the measurements (approximately 10%) a sharp (up to 1012) change in the mobility of hydrogen in the hydrides induced by temperature changes within the ranges indicated does not noticeably affect the probabilities for π- meson capture by bound hydrogen, i.e. does not lead to appreciable changes in the Me-H bond. A comparison of the capture probabilities for palladium hydride and hydrides of neighboring transition metals shows that there are no pronounced anomalies in the Pd-H bond

  19. Advanced chemical hydride-based hydrogen generation/storage system for fuel cell vehicles

    Energy Technology Data Exchange (ETDEWEB)

    Breault, R.W.; Rolfe, J. [Thermo Power Corp., Waltham, MA (United States)

    1998-08-01

    Because of the inherent advantages of high efficiency, environmental acceptability, and high modularity, fuel cells are potentially attractive power supplies. Worldwide concerns over clean environments have revitalized research efforts on developing fuel cell vehicles (FCV). As a result of intensive research efforts, most of the subsystem technology for FCV`s are currently well established. These include: high power density PEM fuel cells, control systems, thermal management technology, and secondary power sources for hybrid operation. For mobile applications, however, supply of hydrogen or fuel for fuel cell operation poses a significant logistic problem. To supply high purity hydrogen for FCV operation, Thermo Power`s Advanced Technology Group is developing an advanced hydrogen storage technology. In this approach, a metal hydride/organic slurry is used as the hydrogen carrier and storage media. At the point of use, high purity hydrogen will be produced by reacting the metal hydride/organic slurry with water. In addition, Thermo Power has conceived the paths for recovery and regeneration of the spent hydride (practically metal hydroxide). The fluid-like nature of the spent hydride/organic slurry will provide a unique opportunity for pumping, transporting, and storing these materials. The final product of the program will be a user-friendly and relatively high energy storage density hydrogen supply system for fuel cell operation. In addition, the spent hydride can relatively easily be collected at the pumping station and regenerated utilizing renewable sources, such as biomass, natural, or coal, at the central processing plants. Therefore, the entire process will be economically favorable and environmentally friendly.

  20. Neutral water-chemical regime with hydrogen peroxide dosage at the AMB-200 unit

    International Nuclear Information System (INIS)

    Results of investigations related to estimation of erosion-corrosion process rates on feed water treatment with hydrogen peroxide at the Beloyarskaya NPP second unit are given. As follows from analysis, values of electric conductivity and iron oxide concentrations reduced two times as compared with correctionless regimes. Metal erosion rate in some feed water loop sections reduced 200-600 times. Hydrogen peroxide metering for feed water provides good condition and reliable operation of feed water loop equipment, reactor circuit and process tubes of the AMB-200 reactor unit

  1. Transformation of biogenic carbohydrates into levulinic acid and further hydrogenation using supported nanoparticle catalysts synthesized by chemical fluid deposition

    OpenAIRE

    Yan, Kai

    2011-01-01

    The primary objective of this thesis was to synthesize and identify powerful metal catalysts and key factors for the conversion of D-fructose and D-glucose to LA as well as the hydrogenation of LA to GVL. A general overview on the use of biomass for chemicals and potential biofuel production is provided. The catalytic transformation systems developed for the conversion of biomass-derived monomers to LA and GVL are reviewed. Meanwhile, an intensive overview of the preparation of supported nano...

  2. Hydrogen production from a chemical cycle of H{sub 2}S splitting

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hui [Department of Chemical Engineering, University of Saskatchewan, Saskatoon, Saskatchewan (Canada)

    2007-11-15

    The sulphur-iodine thermochemical water-splitting cycle (S-I cycle) developed for hydrogen production from water is fundamentally based on the following three chemical reactions: H{sub 2}SO{sub 4}{yields}H{sub 2}O+SO{sub 2}+0.5O{sub 2},2H{sub 2}O+SO{sub 2}+I{sub 2}{yields}H{sub 2}SO{sub 4}+2HI,2HI{yields}H{sub 2}+I{sub 2}.This paper proposes to replace the H{sub 2}SO{sub 4} decomposition with a reaction between H{sub 2}S and H{sub 2}SO{sub 4} and the replacement gives rise to a H{sub 2}S-splitting cycle that produces H{sub 2} and elemental S from H{sub 2}S, shown as follows: H{sub 2}S+H{sub 2}SO{sub 4}{yields} S+SO{sub 2}+2H{sub 2}O,2H{sub 2}O+I{sub 2}+SO{sub 2}{yields}H{sub 2}SO{sub 4}+2HI,2HI{yields}H{sub 2}+I{sub 2}.Combined with the reactions such as O{sub 2}+S{yields}SO{sub 2},SO{sub 2}+0.5O{sub 2}{yields}SO{sub 3},SO{sub 3}+H{sub 2}O{yields}H{sub 2}SO{sub 4},this new cycle cannot only produce more H{sub 2} and extra H{sub 2}SO{sub 4} but also facilitate flexible H{sub 2} to H{sub 2}SO{sub 4} production ratio. Thermodynamic analysis shows that the new cycle is more energy-efficient than the S-I cycle of water-splitting because a series of endothermic reactions in H{sub 2}SO{sub 4} decomposition have been replaced with an exothermic reaction between H{sub 2}S and H{sub 2}SO{sub 4}. Technologies to be developed from this chemistry will be able to convert H{sub 2}S from sour or acid gas into H{sub 2} and elemental S or H{sub 2}SO{sub 4}, which are more valuable than elemental S only, the product of the Claus process. In upgrading and refinery, the H{sub 2} produced can be returned to use in hydrotreating; and in gas plants, H{sub 2} from H{sub 2}S splitting is an alternative clean fuel. Environmentally, H{sub 2} production based on this H{sub 2}S-splitting cycle is carbon free. (author)

  3. 76 FR 69136 - Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting

    Science.gov (United States)

    2011-11-08

    ... required by 1 CFR 21.1, regarding the lifted stay of hydrogen sulfide reporting requirements. In FR Doc... a document on August 22, 1994 (59 FR 43048) imposing stays on the reporting requirements for... Register of October 17, 2011 (76 FR 64022) should have lifted the Administrative Stay of the...

  4. Chemically modified glasses for analysis of hydrogen isotopes by gas chromatography

    International Nuclear Information System (INIS)

    An extensive experimental research has been carried out by gas chromatographic runs in order to identify the most suitable adsorbents and define the best operated conditions for selective separation and analysis of hydrogen isotopes in near real-time (i.e. less than 10 min.). Preparation and operation procedures of chromatographic column for hydrogen isotope separation have been examined. This is one of the main requirements of the tritium separation from heavy water of CANDU reactor and of the tritium fuel cycle in D-T fusion reactors. This paper describes the preparation of absorbent materials utilised as stationary phase in the gas-chromatographic column for hydrogen isotope separation and treatment (activation) of stationary phase. Modified thermoresisting glass with Fe(NH4)2(SO4)2 6H2O and Cr2O3, respectively, have been experimentally investigated at 77 K for H2, HD, and D2 separation and the results of chromatographic runs are also reported and discussed. The hydrogen operating conditions of the adsorbent column Fe (III)/glass and Cr2O3/glass, i.e. granulometry, column length, pressure-drop along the column, carrier gas flow rate, sample volume have been study by means of the analysis of the retention times, separation factors and HETP. (authors)

  5. Lithium borohydride–melamine complex as a promising material for chemical hydrogen storage

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Lin; Hu, Daqiang; He, Teng; Zhang, Yao; Wu, Guotao; Chu, Hailiang; Wang, Peikun [Dalian National Laboratory for Clear Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China); Xiong, Zhitao, E-mail: xzt@dicp.ac.cn [Dalian National Laboratory for Clear Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China); Chen, Ping [Dalian National Laboratory for Clear Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023 (China)

    2013-03-05

    Highlights: ► 3LiBH{sub 4}·C{sub 3}H{sub 6}N{sub 6} was synthesized by ball milling of LiBH{sub 4} and C{sub 3}H{sub 6}N{sub 6}. ► 3LiBH{sub 4}·C{sub 3}N{sub 6}H{sub 6} starts to evolve hydrogen at ca. 100 °C. ► 7.83 wt.% of Hydrogen can be evolved in the temperature range of 100–340 °C. ► Combination reaction between NH and BH can improve dehydrogenation properties. -- Abstract: A complex hydride, 3LiBH{sub 4}·C{sub 3}N{sub 6}H{sub 6}, crystallizing in monoclinic structure with lattice parameters of a = 17.4701 Å, b = 17.6332 Å, c = 4.1749 Å, β = 99.7453° and V = 1267.54 Å{sup 3}, was synthesized by solid reaction between LiBH{sub 4} and C{sub 3}N{sub 6}H{sub 6}. 3LiBH{sub 4}·C{sub 3}N{sub 6}H{sub 6} starts to evolve hydrogen at 100 °C, which is 190 °C lower than that of pristine LiBH{sub 4}. Combination of protic hydrogen of [BH{sub 4}]{sup −} and hydridic hydrogen of NH in 3LiBH{sub 4}·C{sub 3}N{sub 6}H{sub 6} may greatly improve the dehydrogenation properties, and totally 7.83 wt.% H{sub 2} can be released from 3LiBH{sub 4}·C{sub 3}N{sub 6}H{sub 6} in the temperature range of 100–340 °C.

  6. Carbon-supported platinum alloy catalysts for phenol hydrogenation for making industrial chemicals

    Energy Technology Data Exchange (ETDEWEB)

    Srinivas, S.T.; Song, C.

    1999-07-01

    Phenol is available in large quantities in liquids derived from coal and biomass. Phenol hydrogenation is an industrially important reaction to produce cyclohexanone and cyclohexanol. Cyclohexane, cyclohexene and benzene are obtained as minor products in this reaction. Cyclohexanone is an important intermediate in the production of caprolactam for nylon 6 and cyclohexanol for adipic acid production. In USA, cyclohexanol and cyclohexanone are produced by benzene hydrogenation to cyclohexane over nickel or noble metal catalysts, followed by oxidation of cyclohexane to produce a mixture of cyclohexanol and cyclohexanone. Then cyclohexanol is dehydrogenated in the presence of Cu-Zn catalyst to cyclohexanone. Usually phenol hydrogenation is also carried out by using Ni catalyst in liquid phase. However, a direct single-step vapor phase hydrogenation of phenol to give cyclohexanone selectively is more advantageous in terms of energy savings and process economics, since processing is simplified and the endothermic step of cyclohexanol dehydrogenation can be avoided, as demonstrated by Montedipe and Johnson Matthey using promoted Pd/Al{sub 2}O{sub 3} catalyst. While it is not the purpose of this paper to dwell on the relative merits of these routes, it is necessary to mention that while using monometallic catalysts, generally the problem of catalyst deactivation of sintering as well as coking is frequently encountered. Addition and alloying of noble metal (e.g. Pt) with a second metal can result in a catalyst with better selectivity and activity in the reaction which is more resistant to deactivation. This paper presents the results on the single-step vapor phase hydrogenation of phenol over carbon-supported Pt-M (M=Cr, V, Zr) alloy catalysts to yield mainly cyclohexanone or cyclohexanol.

  7. Influence of density on radiation-chemical yield of molecular hydrogen formed at radiolysis of aqueous solution of NaOH

    International Nuclear Information System (INIS)

    Full text : In atom and nuclear energy the specialists knowledge about radiation-chemical yield of the initial products formed under the influence of ionizing rays on water is of great importance from the point of security. The radiation-chemical yields of molecular hydrogen have been defined according to the graph and the obtained results

  8. Chemical Reactivity Dynamics and Quantum Chaos in Highly Excited Hydrogen Atoms in an External Field: A Quantum Potential Approach

    Directory of Open Access Journals (Sweden)

    B. Maiti

    2002-04-01

    Full Text Available Abstract: Dynamical behavior of chemical reactivity indices like electronegativity, hardness, polarizability, electrophilicity and nucleophilicity indices is studied within a quantum fluid density functional framework for the interactions of a hydrogen atom in its ground electronic state (n = 1 and an excited electronic state (n = 20 with monochromatic and bichromatic laser pulses. Time dependent analogues of various electronic structure principles like the principles of electronegativity equalization, maximum hardness, minimum polarizability and maximum entropy have been found to be operative. Insights into the variation of intensities of the generated higher order harmonics on the color of the external laser field are obtained. The quantum signature of chaos in hydrogen atom has been studied using a quantum theory of motion and quantum fluid dynamics. A hydrogen atom in the electronic ground state (n = 1 and in an excited electronic state ( n = 20 behaves differently when placed in external oscillating monochromatic and bichromatic electric fields. Temporal evolutions of Shannon entropy, quantum Lyapunov exponent and Kolmogorov – Sinai entropy defined in terms of the distance between two initially close Bohmian trajectories for these two cases show marked differences. It appears that a larger uncertainty product and a smaller hardness value signal a chaotic behavior.

  9. Electron-electron interactions in the chemical bond: ``1/3” Effect in the bond length of hydrogen molecule

    Indian Academy of Sciences (India)

    P Ganguly

    2001-10-01

    The prominent ``1/3” effect observed in the Hall effect plateaus of twodimensional electron gas (2DEG) systems has been postulated to indicating 1/3 fractional charge quasiparticle excitations arising from electron-electron interactions. Tunneling shot-noise experiments on 2DEF exhibiting fractional quantum Hall effect (FQHE) shows evidence for tunnelling of particles with and /3 charges for a constant band mass. A ``1/3” effect in the hydrogen molecule is seen in as much as its internuclear distance, - = - + +, with |+/-| = 1/3. This is examined in terms of electron-electron interactions involving electron- and hole quasiparticles, (-) and (ℎ+), equivalent to those observed in FQHE shot-noise experiments. The (/) ratio of the (-) and (ℎ+) quasiparticles is kept at 1: -3. Instead of a 2DEG, these particles are treated as being in flat Bohr orbits. A treatment in the language of charge-flux tube composites for the hydrogen atom as well as the hydrogen molecule is attempted. Such treatment gives important insights into changes in chemical potential and bond energy on crossing a phase boundary during the atom-bond transition as well as on models for FQHE itself.

  10. Research on the Interaction of Hydrogen-Bond Acidic Polymer Sensitive Sensor Materials with Chemical Warfare Agents Simulants by Inverse Gas Chromatography

    Directory of Open Access Journals (Sweden)

    Liu Yang

    2015-06-01

    Full Text Available Hydrogen-bond acidic polymers are important high affinity materials sensitive to organophosphates in the chemical warfare agent sensor detection process. Interactions between the sensor sensitive materials and chemical warfare agent simulants were studied by inverse gas chromatography. Hydrogen bonded acidic polymers, i.e., BSP3, were prepared for micro-packed columns to examine the interaction. DMMP (a nerve gas simulant and 2-CEES (a blister agent simulant were used as probes. Chemical and physical parameters such as heats of absorption and Henry constants of the polymers to DMMP and 2-CEES were determined by inverse gas chromatography. Details concerning absorption performance are also discussed in this paper.

  11. Catalytic Lignin Valorization Process for the Production of Aromatic Chemicals and Hydrogen

    NARCIS (Netherlands)

    Zakzeski, J.; Jongerius, A.L.; Bruijnincx, P.C.A.; Weckhuysen, B.M.

    2012-01-01

    With dwindling reserves of fossil feedstock as a resource for chemicals production, the fraction of chemicals and energy supplied by alternative, renewable resources, such as lignin, can be expected to increase in the foreseeable future. Here, we demonstrate a catalytic process to valorize lignin (e

  12. ECF BLEACHING WITH A FINAL HYDROGEN PEROXIDE STAGE: IMPACT ON THE CHEMICAL COMPOSITION OF Eucalyptus globulus KRAFT PULPS

    Directory of Open Access Journals (Sweden)

    Pedro E. G. Loureiro

    2010-11-01

    Full Text Available Two industrial elemental chlorine free (ECF bleaching sequences, D0(EOPD1(EPD2 and OQ(PODP, are compared with respect to the bulk content of lignin, carboxyl, hexeneuronic acids (HexA, and reducing groups after each bleaching stage. HexA groups contribute significantly to the total content of carboxyl groups, and their degradation during chlorine dioxide bleaching is reflected by a decrease of the carboxyl content. The higher degradation using an enhanced use of oxygen-based bleaching chemicals is associated with a higher fiber charge reduction, mainly due to xylan depletion. Additionally, the effect of process variables of a laboratory final hydrogen peroxide stage on the chemical composition of the fully bleached pulp (D0(EOPD1P and OQ(PODP is studied. The ability of final peroxide bleaching to raise the content of carboxyl groups is dependent on the operating conditions and pulp bleaching history. A balance between carbohydrate oxidation and dissolution of oxidized groups determines the effect on fiber charge. The effect of hydrogen peroxide stabilizers added into the final stage on the content of carboxyl groups is also reported.

  13. CH spectroscopy for carbon chemical erosion analysis in high density low temperature hydrogen plasma

    NARCIS (Netherlands)

    Westerhout, J.; Cardozo, N. J. L.; Rapp, J.; van Rooij, G. J.

    2009-01-01

    The CH A-X molecular band is measured upon seeding the hydrogen plasma in the linear plasma generator Pilot-PSI [electron temperature T-e=0.1-2.5 eV and electron density n(e)=(0.5-5) X 10(20) m(-3)] with methane. Calculated inverse photon efficiencies for these conditions range from 3 up to >10(6

  14. Phytotoxic cyanamide affects maize (Zea mays) root growth and root tip function: from structure to gene expression.

    Science.gov (United States)

    Soltys, Dorota; Rudzińska-Langwald, Anna; Kurek, Wojciech; Szajko, Katarzyna; Sliwinska, Elwira; Bogatek, Renata; Gniazdowska, Agnieszka

    2014-05-01

    Cyanamide (CA) is a phytotoxic compound produced by four Fabaceae species: hairy vetch, bird vetch, purple vetch and black locust. Its toxicity is due to complex activity that involves the modification of both cellular structures and physiological processes. To date, CA has been investigated mainly in dicot plants. The goal of this study was to investigate the effects of CA in the restriction of the root growth of maize (Zea mays), representing the monocot species. CA (3mM) reduced the number of border cells in the root tips of maize seedlings and degraded their protoplasts. However, CA did not induce any significant changes in the organelle structure of other root cells, apart from increased vacuolization. CA toxicity was also demonstrated by its effect on cell cycle activity, endoreduplication intensity, and modifications of cyclins CycA2, CycD2, and histone HisH3 gene expression. In contrast, the arrangement of microtubules was not altered by CA. Treatment of maize seedlings with CA did not completely arrest mitotic activity, although the frequency of dividing cells was reduced. Furthermore, prolonged CA treatment increased the proportion of endopolyploid cells in the root tip. Cytological malformations were accompanied by an induction of oxidative stress in root cells, which manifested as enhanced accumulation of H2O2. Exposure of maize seedlings to CA resulted in an increased concentration of auxin and stimulated ethylene emission. Taken together, these findings suggested that the inhibition of root growth by CA may be a consequence of stress-induced morphogenic responses.

  15. Chemisorption of hydrogen and oxygen atoms on a cobalt surface: A quantum chemical cluster model study

    International Nuclear Information System (INIS)

    The chemisorption of atomic hydrogen and oxygen on a cobalt surface has been studied on a five-atom cluster model using one-electron effective core potential (le- ECP) and all-electron calculations at the ab initio SCF and MCPF levels. Also, density functional calculations have been carried out. The different approaches are evaluated. The le- ECP has been compared to similar ECPS for nickel and copper. Our results indicate that this approach is valid also for cobalt. Different contributions to the cluster-adsorbate bonding energy are discussed. 31 refs., 1 fig., 1 tab

  16. Chemical Looping Gasification for Hydrogen Enhanced Syngas Production with In-Situ CO2 Capture

    Energy Technology Data Exchange (ETDEWEB)

    Kathe, Mandar [Ohio State University, Columbus, OH (United States); Xu, Dikai [Ohio State University, Columbus, OH (United States); Hsieh, Tien-Lin [Ohio State University, Columbus, OH (United States); Simpson, James [Ohio State University, Columbus, OH (United States); Statnick, Robert [Ohio State University, Columbus, OH (United States); Tong, Andrew [Ohio State University, Columbus, OH (United States); Fan, Liang-Shih [Ohio State University, Columbus, OH (United States)

    2014-12-31

    This document is the final report for the project titled “Chemical Looping Gasification for Hydrogen Enhanced Syngas Production with In-Situ CO2 Capture” under award number FE0012136 for the performance period 10/01/2013 to 12/31/2014.This project investigates the novel Ohio State chemical looping gasification technology for high efficiency, cost efficiency coal gasification for IGCC and methanol production application. The project developed an optimized oxygen carrier composition, demonstrated the feasibility of the concept and completed cold-flow model studies. WorleyParsons completed a techno-economic analysis which showed that for a coal only feed with carbon capture, the OSU CLG technology reduced the methanol required selling price by 21%, lowered the capital costs by 28%, increased coal consumption efficiency by 14%. Further, using the Ohio State Chemical Looping Gasification technology resulted in a methanol required selling price which was lower than the reference non-capture case.

  17. Influence of hydrogen dilution on structural, electrical and optical properties of hydrogenated nanocrystalline silicon (nc-Si:H) thin films prepared by plasma enhanced chemical vapour deposition (PE-CVD)

    Energy Technology Data Exchange (ETDEWEB)

    Funde, A.M.; Bakr, Nabeel Ali; Kamble, D.K. [School of Energy Studies, University of Pune, Pune 411 007 (India); Hawaldar, R.R.; Amalnerkar, D.P. [Center for Materials for Electronics Technology (C-MET), Panchawati, Pune 411 008 (India); Jadkar, S.R. [Department of Physics, University of Pune, Ganeshkhind Road, Pune 411 007 (India)

    2008-10-15

    Hydrogenated nanocrystalline silicon (nc-Si:H) thin films were deposited from pure silane (SiH{sub 4}) and hydrogen (H{sub 2}) gas mixture by conventional plasma enhanced chemical vapour deposition (PE-CVD) method at low temperature (200 C) using high rf power. The structural, optical and electrical properties of these films are carefully and systematically investigated as a function of hydrogen dilution of silane (R). Characterization of these films with low angle X-ray diffraction and Raman spectroscopy revealed that the crystallite size in the films tends to decrease and at same time the volume fraction of crystallites increases with increase in R. The Fourier transform infrared (FTIR) spectroscopic analysis showed at low values of R, the hydrogen is predominantly incorporated in the nc-Si:H films in the mono-hydrogen (Si-H) bonding configuration. However, with increasing R the hydrogen bonding in nc-Si:H films shifts from mono-hydrogen (Si-H) to di-hydrogen (Si-H{sub 2}) and (Si-H{sub 2}){sub n} complexes. The hydrogen content in the nc-Si:H films decreases with increase in R and was found less than 10 at% over the entire studied range of R. On the other hand, the Tauc's optical band gap remains as high as 2 eV or much higher. The quantum size effect may responsible for higher band gap in nc-Si:H films. A correlation between electrical and structural properties has been found. For optimized deposition conditions, nc-Si:H films with crystallite size {proportional_to}7.67 nm having good degree of crystallinity ({proportional_to}84%) and high band gap (2.25 eV) were obtained with a low hydrogen content (6.5 at%). However, for these optimized conditions, the deposition rate was quite small (1.6 Aa/s). (author)

  18. Hydrogenation of biomass extracts for production of chemicals concurrently from sugars and lignin

    Science.gov (United States)

    The efficient conversion of biomass to commodity or specialty chemicals is critical to the success of the biorefinery concept. Biomass consists largely of the three interwoven polymers cellulose, hemicellulose, and lignin [1]. A key step toward utilization is the pretreatment of biomass which includ...

  19. Cobalt (hydr)oxide/graphite oxide composites: importance of surface chemical heterogeneity for reactive adsorption of hydrogen sulfide.

    Science.gov (United States)

    Mabayoje, Oluwaniyi; Seredych, Mykola; Bandosz, Teresa J

    2012-07-15

    Composites of cobalt (hydr)oxide and graphite oxide (GO) were obtained and evaluated as adsorbents of hydrogen sulfide at ambient conditions. The surface properties of the initial and exhausted samples were studied by FTIR, TEM, SEM/EDX, XRD, adsorption of nitrogen, potentiometric titration, and thermal analysis. The results obtained show a significant improvement in their adsorption capacities compared to parent compounds. The importance of the OH groups of cobalt (hydr)oxide/GO composites and new interface chemistry for the adsorption of hydrogen sulfide on these materials is revealed. The oxygen activation by the carbonaceous component resulted in formation of sulfites. Water enhanced the removal process. This is the result of the basic environment promoting dissociation of H(2)S and acid-base reactions. Finally, the differences in the performance of the materials with different mass ratios of GO were linked to the availability of active sites on the surface of the adsorbents, dispersion of these sites, their chemical heterogeneity, and location in the pore system.

  20. Chemical vapor deposition of monolayer WS2 nano- sheets on Au foils toward direct application in hydrogen evolution

    Institute of Scientific and Technical Information of China (English)

    Yanshuo Zhang[1; Jianping Shi[1; Gaofeng Han[3; Minjie Li[2; Qingqing Ji[2; Donglin Ma[2; Yu Zhang[1,2; Cong Li[1,2; Xingyou Lang[3; Yanfeng Zhang[1,2; Zhongfan Liu[2

    2015-01-01

    Monolayer tungsten disulfide (WS2), a typical member of the semiconducting transition metal dichalcogenide family has drawn considerable interest because of its unique properties. Intriguingly the edge of WS2 exhibits an ideal hydrogen binding energy which makes WS2 a potential alternative to Pt-based electrocatalysts for the hydrogen evolution reaction (HER). Here, we demonstrate for the first time the successful synthesis of uniform monolayer WS2 nanosheets on centimeter- scale Au foils using a facile, low-pressure chemical vapor deposition method. The edge lengths of the universally observed triangular WS2 nanosheets are tunable from -100 to N1,000 nm. The WS2 nanosheets on Au foils featuring abundant edges were then discovered to be efficient catalysts for the HER, exhibiting a rather high exchange current density of -30.20 μA/cm2 and a small onset potential of Nl10 mV. The effects of coverage and domain size (which correlate closely with the active edge density of WS2) on the electrocatalytic activity were investigated. This work not only provides a novel route toward the batch-production of monolayer WS2 via the introduction of metal foil substrates but also opens up its direct application for facile HER.

  1. Ultrasound promoted catalytic liquid-phase dehydrogenation of isopropanol for Isopropanol-Acetone-Hydrogen chemical heat pump.

    Science.gov (United States)

    Xu, Min; Xin, Fang; Li, Xunfeng; Huai, Xiulan; Liu, Hui

    2015-03-01

    The apparent kinetic of the ultrasound assisted liquid-phase dehydrogenation of isopropanol over Raney nickel catalyst was determined in the temperature range of 346-353 K. Comparison of the effects of ultrasound and mechanical agitation on the isopropanol dehydrogenation was investigated. The ultrasound assisted dehydrogenation rate was significantly improved when relatively high power density was used. Moreover, the Isopropanol-Acetone-Hydrogen chemical heat pump (IAH-CHP) with ultrasound irradiation, in which the endothermic reaction is exposure to ultrasound, was proposed. A mathematical model was established to evaluate its energy performance in term of the coefficient of performance (COP) and the exergy efficiency, into which the apparent kinetic obtained in this work was incorporated. The operating performances between IAH-CHP with ultrasound and mechanical agitation were compared. The results indicated that the superiority of the IAH-CHP system with ultrasound was present even if more than 50% of the power of the ultrasound equipment was lost.

  2. Stress relief patterns of hydrogenated amorphous carbon films grown by dc-pulse plasma chemical vapor deposition

    Science.gov (United States)

    Wang, Qi; Wang, Chengbing; Wang, Zhou; Zhang, Junyan; He, Deyan

    2008-12-01

    Hydrogenated amorphous carbon films were prepared on Si (1 0 0) substrates by dc-pulse plasma chemical vapor deposition. The nature of the deposited films was characterized by Raman spectra and the stress relief patterns were observed by scanning electron microscope. Besides the well-known sinusoidal type and flower type patterns, etc., two different stress relief patterns, ring type and peg-top shape with exiguous tine on the top, were observed. The ring type in this paper was a clear ridge-cracked buckle and unusual. Two competing buckle delamination morphologies ring and sinusoidal buckling coexist. The ridge-cracked buckle in ring type was narrower than the sinusoidal buckling. Meanwhile peg-top shape with exiguous tine on the top in this paper was unusual. These different patterns supported the approach in which the stress relief forms have been analyzed using the theory of plate buckling.

  3. Electroless chemical grafting of nitrophenyl groups on n-doped hydrogenated amorphous silicon surfaces.

    Science.gov (United States)

    Kim, Chulki; Oh, Kiwon; Han, Seunghee; Kim, Kyungkon; Kim, Il Won; Kim, Heesuk

    2014-08-01

    The direct spontaneous grafting of 4-nitrophenyl molecules onto n-doped hydrogenated amorphous silicon (a-Si:H) surfaces without external ultraviolet, thermal, or electrochemical energy was invegtigated. Clean n-doped a-Si:H thin films were dipped in a solution of 4-nitrobenzenediazonium salts (PNBD) in acetonitrile. After the modified surfaces were rinsed, they were analyzed qualitatively and quantitatively by X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). XPS and AFM results show that the reaction of an n-doped a-Si:H thin film with PNBD self-terminates without polymerization, after 5 h, and the surface number density of 4-nitrophenyl molecules is 4.2 x 10(15)/cm2. These results demonstrate that the spontaneous grafting of nitrophenyl layers onto n-doped a-Si:H thin films is an attractive pathway toward forming interfaces between a-Si:H and organic layers under ambient conditions. PMID:25936109

  4. Hydrogen Safety Project chemical analysis support task: Window ``C`` volatile organic analysis

    Energy Technology Data Exchange (ETDEWEB)

    Gillespie, B.M.; Stromatt, R.W.; Ross, G.A.; Hoope, E.A.

    1992-01-01

    This data package contains the results obtained by Pacific Northwest Laboratory (PNL) staff in the characterization of samples for the 101-SY Hydrogen Safety Project. The samples were submitted for analysis by Westinghouse Hanford Company (WHC) under the Technical Project Plan (TPP) 17667 and the Quality Assurance Plan MCS-027. They came from a core taken during Window ``C`` after the May 1991 gas release event. The analytical procedures required for analysis were defined in the Test Instructions (TI) prepared by the PNL 101-SY Analytical Chemistry Laboratory (ACL) Project Management Office in accordance with the TPP and the QA Plan. The requested analysis for these samples was volatile organic analysis. The quality control (QC) requirements for each sample are defined in the Test Instructions for each sample. The QC requirements outlined in the procedures and requested in the WHC statement of work were followed.

  5. Hydrogen Safety Project chemical analysis support task: Window C'' volatile organic analysis

    Energy Technology Data Exchange (ETDEWEB)

    Gillespie, B.M.; Stromatt, R.W.; Ross, G.A.; Hoope, E.A.

    1992-01-01

    This data package contains the results obtained by Pacific Northwest Laboratory (PNL) staff in the characterization of samples for the 101-SY Hydrogen Safety Project. The samples were submitted for analysis by Westinghouse Hanford Company (WHC) under the Technical Project Plan (TPP) 17667 and the Quality Assurance Plan MCS-027. They came from a core taken during Window C'' after the May 1991 gas release event. The analytical procedures required for analysis were defined in the Test Instructions (TI) prepared by the PNL 101-SY Analytical Chemistry Laboratory (ACL) Project Management Office in accordance with the TPP and the QA Plan. The requested analysis for these samples was volatile organic analysis. The quality control (QC) requirements for each sample are defined in the Test Instructions for each sample. The QC requirements outlined in the procedures and requested in the WHC statement of work were followed.

  6. Effects of chemical coating with Ni on electrochemical properties of Mg2Ni hydrogen storage alloys

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The effects of nickel coating on the electrochemical properties of Mg2Ni hydrogen storage alloys are presented in this paper. X-ray diffraction (XRD) and scanning electron microscope (SEM) techniques were employed to examine the crystal structure and surface morphologies of the bare and Ni-coated Mg2Ni alloys. The electrochemical properties of alloys were characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results showed that Ni coating not only decreased the charge transfer resistance, but also decreased the H atom diflusion resistance for Mg2Ni alloys. It was also found that Ni coating effectively improved the discharge capacity, but decreased the cycling performance of the as-synthesized Ni-coated Mg2Ni alloys. The discharge current has a great impact on the cycling performance of the as-synthesized Ni-coated Mg2Ni alloys.

  7. Efeito da aplicação de cianamida hidrogenada e óleo mineral na quebra de dormência e producão do pessegueiro-'Flamecrest' Effect of the application of hidrogen cyanamid and mineral oil on dormancy breaking and peach production, cv. Flamecrest

    Directory of Open Access Journals (Sweden)

    GILMAR ARDUINO BETTIO MARODIN

    2002-08-01

    August. The Dormancy breaking, flowering, fruit set, yield, and antecipation of harvest were evaluated from plants of the folllowing treatments: 1,22; 2,45; 3,675 or 4,90 g of i.a.L-1 hydrogen cyanamid together with 10 g i.a L-1 of mineral oil or a single application of 10 g i.a L-1 mineral oil. The Control plants were not sprayed with the dormancy breaking treatment. None of the treatments resulted in sprouting antecipation of flowering buds however, plants treated with 1,22 or 4,90 g i.a L-1 hydrogen cyanamid mixed with 10 g i.a L-1 mineral oil, had a higher number of sprouted vegetative buds. There was no significant effect of the period of application on flowering and fruit set. The number of fruits thinned out from each plant was higher for the treatments with 2,45 or 4,90 g i.a L-1 of hydrogen cyanamid mixed with 10 g i.a L-1 of mineral oil. When applied to peaches trees in july, the treatments with 1,22 and 3,675 g i.a. L-1 of hydragen cyanamid and 10 g i.a. L-1 of mineral oil resulted in a higher number of fruits and total yield per plant. All the treatments, in the second apllication period, produced higher yields. The Average fruit weight, total soluble solids and pulp firmness were not influenced by the treatments.

  8. Studies on the preparation of active oxygen-deficient copper ferrite and its application for hydrogen production through thermal chemical water splitting

    Institute of Scientific and Technical Information of China (English)

    YU Bo; ZHANG Ping; ZHANG Lei; CHEN Jing; XU JingMing

    2008-01-01

    Hydrogen generation through thermal chemical water splitting technology has recently received in-creasingly international interest in the nuclear hydrogen production field. Besides the main known sulfur-iodine (S-I) cycle developed by the General Atomics Company and the UT3 cycle (iron, calcium, and bromine) developed at the University of Tokyo, the thermal cycle based on metal oxide two-step water splitting methods is also receiving research and development attention worldwide. In this work, copper ferrite was prepared by the co-precipitation method and oxygen-deficient copper ferrite was synthesized through first and second calcination steps for the application of hydrogen production by a two-step water splitting process. The crystal structure, properties, chemical composition and δwere investigated in detail by utilizing X-ray diffraction (XRD), thermogravimetry (TG) and differential thermal analysis (DTA), atomic absorption spectrometer (AAS), ultraviolet spectrophotometry (UV), gas chro-matography (GC), and so on. The experimental two-step thermal chemical cycle reactor for hydrogen generation was designed and developed in this lab. The hydrogen generation process of water splitting through CuFe2O4-δ and the cycle performance of copper ferrite regeneration were firstly studied and discussed.

  9. Studies on the preparation of active oxygen-deficient copper ferrite and its application for hydrogen production through thermal chemical water splitting

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Hydrogen generation through thermal chemical water splitting technology has recently received in- creasingly international interest in the nuclear hydrogen production field. Besides the main known sulfur-iodine (S-I) cycle developed by the General Atomics Company and the UT3 cycle (iron, calcium, and bromine) developed at the University of Tokyo, the thermal cycle based on metal oxide two-step water splitting methods is also receiving research and development attention worldwide. In this work, copper ferrite was prepared by the co-precipitation method and oxygen-deficient copper ferrite was synthesized through first and second calcination steps for the application of hydrogen production by a two-step water splitting process. The crystal structure, properties, chemical composition and δ were investigated in detail by utilizing X-ray diffraction (XRD), thermogravimetry (TG) and differential thermal analysis (DTA), atomic absorption spectrometer (AAS), ultraviolet spectrophotometry (UV), gas chro- matography (GC), and so on. The experimental two-step thermal chemical cycle reactor for hydrogen generation was designed and developed in this lab. The hydrogen generation process of water splitting through CuFe2O4-δ and the cycle performance of copper ferrite regeneration were firstly studied and discussed.

  10. Well-controlled metal co-catalysts synthesised by chemical vapour impregnation for photocatalytic hydrogen production and water purification.

    Science.gov (United States)

    Su, Ren; Forde, Michael M; He, Qian; Shen, Yanbin; Wang, Xueqin; Dimitratos, Nikolaos; Wendt, Stefan; Huang, Yudong; Iversen, Bo B; Kiely, Christopher J; Besenbacher, Flemming; Hutchings, Graham J

    2014-10-28

    As co-catalyst materials, metal nanoparticles (NPs) play crucial roles in heterogeneous photocatalysis. The photocatalytic performance strongly relies on the physical properties (i.e., composition, microstructure, and surface impurities) of the metal NPs. Here we report a convenient chemical vapour impregnation (CVI) approach for the deposition of monometallic-, alloyed, and core-shell structured metal co-catalysts onto the TiO2 photocatalyst. The as-synthesised metal NPs are highly dispersed on the support and show narrow size distributions, which suit photocatalysis applications. More importantly, the surfaces of the as-synthesised metal NPs are free of protecting ligands, enabling the photocatalysts to be ready to use without further treatment. The effect of the metal identity, the alloy chemical composition, and the microstructure on the photocatalytic performance has been investigated for hydrogen production and phenol decomposition. Whilst the photocatalytic H2 production performance can be greatly enhanced by using the core-shell structured co-catalyst (Pdshell-Aucore and Ptshell-Aucore), the Ptshell-Aucore modified TiO2 yields enhanced quantum efficiency but a reduced effective decomposition of phenol to CO2 compared to that of the monometallic counterparts. We consider the CVI approach provides a feasible and elegant process for the decoration of photocatalyst materials. PMID:24970298

  11. Fast synthesis of high-performance graphene films by hydrogen-free rapid thermal chemical vapor deposition.

    Science.gov (United States)

    Ryu, Jaechul; Kim, Youngsoo; Won, Dongkwan; Kim, Nayoung; Park, Jin Sung; Lee, Eun-Kyu; Cho, Donyub; Cho, Sung-Pyo; Kim, Sang Jin; Ryu, Gyeong Hee; Shin, Hae-A-Seul; Lee, Zonghoon; Hong, Byung Hee; Cho, Seungmin

    2014-01-28

    The practical use of graphene in consumer electronics has not been demonstrated since the size, uniformity, and reliability problems are yet to be solved to satisfy industrial standards. Here we report mass-produced graphene films synthesized by hydrogen-free rapid thermal chemical vapor deposition (RT-CVD), roll-to-roll etching, and transfer methods, which enabled faster and larger production of homogeneous graphene films over 400 × 300 mm(2) area with a sheet resistance of 249 ± 17 Ω/sq without additional doping. The properties of RT-CVD graphene have been carefully characterized by high-resolution transmission electron microscopy, Raman spectroscopy, chemical grain boundary analysis, and various electrical device measurements, showing excellent uniformity and stability. In particular, we found no significant correlation between graphene domain sizes and electrical conductivity, unlike previous theoretical expectations for nanoscale graphene domains. Finally, the actual application of the RT-CVD films to capacitive multitouch devices installed in the most sophisticated mobile phone was demonstrated. PMID:24358985

  12. Thermodynamic analysis of SCW NPP cycles with thermo-chemical co-generation of hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Naidin, N.; Mokry, S.; Monichan, R.; Chophla, K.; Pioro, I. [Faculty of Energy Systems and Nuclear Science, Univ. of Ontario Inst. of Technology, Oshawa, Ontario (Canada)], E-mail: Maria.Naidin@mycampus.uoit.ca, Sarah.Mokry@mycampus.uoit.ca, Romson.Monichan@uoit.ca, Karan.Chophla@mycampus.uoit.ca, Igor.Pioro@uoit.ca; Naterer, G.; Gabriel, K. [Faculty of Engineering and Applied Science, Univ. of Ontario Inst. of Technology, Oshawa, Ontario (Canada)], E-mail: Greg.Naterer@uoit.ca, Kamiel.Gabriel@uoit.ca

    2009-07-01

    Research activities are currently conducted worldwide to develop Generation IV nuclear reactor concepts with the objective of improving thermal efficiency and increasing economic competitiveness of Generation IV Nuclear Power Plants (NPPs) compared to modern thermal power plants. The Super-Critical Water-cooled Reactor (SCWR) concept is one of the six Generation IV options chosen for further investigation and development in several countries including Canada and Russia. Water-cooled reactors operating at subcritical pressures (10 - 16 MPa) have provided a significant amount of electricity production for the past 50 years. However, the thermal efficiency of the current NPPs is not very high (30 - 35%). As such, more competitive designs, with higher thermal efficiencies, which will be close to that of modern thermal power plants (45 - 50%), need to be developed and implemented. Super-Critical Water (SCW) NPPs will have much higher operating parameters compared to current NPPs (i.e., steam pressures of about 25 MPa and steam outlet temperatures up to 625{sup o}C). Furthermore, SCWRs operating at higher temperatures can facilitate an economical co-generation of hydrogen through thermochemical cycles (particularly, the copper-chlorine cycle) or direct high-temperature electrolysis. The two SCW NPP cycles proposed by this paper are based on direct, regenerative, no-reheat and single-reheat configurations. As such, the main parameters and performance in terms of thermal efficiency of the SCW NPP concepts mentioned above are being analyzed. The cycles are generally comprised of: an SCWR, a SC turbine, one deaerator, ten feedwater heaters, and pumps. The SC turbine of the no-reheat cycle consists of one High-Pressure (HP) cylinder and two Low-Pressure (LP) cylinders. Alternatively, the SC turbine for the single-reheat cycle is comprised of one High-Pressure (HP) cylinder, one Intermediate-Pressure (IP) cylinder and two Low-Pressure (LP) cylinders. Since the single

  13. A study of the chemical, mechanical, and surface properties of thin films of hydrogenated amorphous carbon

    Energy Technology Data Exchange (ETDEWEB)

    Vandentop, G.J.

    1990-07-01

    Amorphous hydrogenated carbon (a-C:H) films were studied with the objective of elucidating the nucleation and growth mechanisms, and the origin of their unique physical properties. The films were deposited onto Si(100) substrates both on the powered (negatively self-biased) and on the grounded electrodes from methane in an rf plasma (13.56 MHz) at 65 mTorr and 300 to 370 K. The films produced at the powered electrode exhibited superior mechanical properties, such as high hardness. A mass spectrometer was used to identify neutral species and positive ions incident on the electrodes from the plasma, and also to measure ion energies. The effect of varying ion energy flux on the properties of a-C:H films was investigated using a novel pulsed biasing technique. It was demonstrated that ions were not the dominant deposition species as the total ion flux measured was insufficient to account for the observed deposition rate. The interface between thin films of a-C:H and silicon substrates was investigated using angle resolved x-ray photoelectron spectroscopy. A silicon carbide layer was detected at the interface of a hard a-C:H film formed at the powered electrode. At the grounded electrode, where the kinetic energy is low, no interfacial carbide layer was observed. Scanning tunneling microscopy and high energy electron energy loss spectroscopy was used to investigate the initial stages of growth of a-C:H films. On graphite substrates, films formed at the powered electrode were observed to nucleate in clusters approximately 50 {Angstrom} in diameter, while at the grounded electrode no cluster formation was observed. 58 figs.

  14. Chemical engineering challenges in driving thermochemical hydrogen processes with the tandem mirror reactor

    International Nuclear Information System (INIS)

    The Tandem Mirror Reactor is described and compared with Tokamaks, both from a basic physics viewpoint and from the suitability of the respective reactor for synfuel production. Differences and similarities between the TMR as an electricity producer or a synfuel producer are also cited. The Thermochemical cycle chosen to link with the fusion energy source is the General Atomic Sulfur-Iodine Cycle, which is a purely thermal-driven process with no electrochemical steps. There are real chemical engineering challenges of getting this high quality heat into the large thermochemical plant in an efficient manner. We illustrate with some of our approaches to providing process heat via liquid sodium to drive a 1050 K, highly-endothermic, catalytic and fluidized-bed SO3 Decomposition Reactor. The technical, economic, and safety tradeoffs that arise are discussed

  15. Combination moisture and hydrogen getter

    Science.gov (United States)

    Harrah, L.A.; Mead, K.E.; Smith, H.M.

    1983-09-20

    A combination moisture and hydrogen getter comprises (a) a moisture getter comprising a readily oxidizable metal; and (b) a hydrogen getter comprising (1) a solid acetylenic compound and (2) a hydrogenation catalyst. A method of scavenging moisture from a closed container uses the combination moisture and hydrogen getter to irreversibly chemically reduce the moisture and chemically bind the resultant hydrogen.

  16. Integrated chemical treatment of municipal wastewater using waste hydrogen peroxide and ultraviolet light

    Science.gov (United States)

    Bhatti, Zulfiqar Ahmed; Mahmood, Qaisar; Raja, Iftikhar Ahmad; Malik, Amir Haider; Rashid, Naim; Wu, Donglei

    Dilemmas like water shortage, rapid industrialization, growing human population and related issues have seriously affected human health and environmental sustainability. For conservation and sustainable use of our water resources, innovative methods for wastewater treatment are continuously being explored. Advance Oxidation Processes (AOPs) show a promising approach to meet specific objectives of municipal wastewater treatment (MWW). The MWW samples were pretreated with Al 2(SO 4) 4·8H 2O (Alum) at different doses 4, 8, 12-50 mg/L to enhance the sedimentation. The maximum COD removal was observed at alum treatments in range of 28-32 mg/L without increasing total dissolved solids (TDS). TDS were found to increase when the alum dose was increased from 32-40 mg/L. In the present study, the optimum alum dose of 30 mg/L for 3 h of sedimentation and subsequent integrated H 2O 2/UV treatment was applied (using 2.5 mL/L of 40% waste H 2O 2 and 35% fresh H 2O 2 separately). Organic and inorganic pollutants, contributing towards chemical oxygen demand (COD), biological oxygen demand (BOD), turbidity and total dissolved solids were degraded by H 2O 2/UV. About 93% COD, 90% BOD and 83% turbidity reduction occurred when 40% waste H 2O 2 was used. When using fresh H 2O 2, 63% COD, 68% BOD and 86% turbidity reduction was detected. Complete disinfection of coliform bacteria occurred by using 40% H 2O 2/UV. The most interesting part of this research was to compare the effectiveness of waste H 2O 2 with fresh H 2O 2. Waste H 2O 2 generated from an industrial process of disinfection was found more effective in the treatment of MWW than fresh 35% H 2O 2.

  17. Regulation of manganese peroxidase gene transcription by hydrogen peroxide, chemical stress, and molecular oxygen

    Energy Technology Data Exchange (ETDEWEB)

    Li, D.; Alic, M.; Brown, J.A.; Gold, M.H. [Oregon Graduate Institute of Science and Technology, Portland, OR (United States)

    1995-01-01

    The expression of manganese peroxidase (MnP) in nitrogen-limited cultures of the lignin-degrading fungus Phanerochaete chrysosporium is regulated at the level of gene transcription by H{sub 2}O{sub 2} and various chemicals, including ethanol, sodium arsenite, and 2,4-dichlorophenol, as well as by Mn(II) and heat shock. Northern (RNA) blot analysis demonstrates that the addition of 1.0 mM H{sub 2}O{sub 2} to 5-day-old cultures grown in the absence of Mn results in the appearance of mnp mRNA within 15 min. Higher levels of mnp mRNA are obtained with simultaneous induction by Mn and H{sub 2}O{sub 2} than with H{sub 2}O{sub 2} alone. Although neither MnP activity nor associated protein is detectable in H{sub 2}O{sub 2}-induced cultures grown in the absence of Mn, simultaneous induction with Mn and H{sub 2}O{sub 2} results in a 1.6-fold increase in MnP activity compared with the MnP activity resulting resulting from Mn induction alone. In the presence of Mn, purging of low-nitrogen cultures with 100% O{sub 2}, in contrast to incubation under air, results in an increase in the accumulation of mnp mRNA and a 13-fold increase in MnP activity on day 5. However, in contrast to the effects of H{sub 2}O{sub 2} and heat shock, O{sub 2} purging of Mn-deficient cultures results in negligible accumulation of mnp mRNA. 48 refs., 6 figs.

  18. The hydrogen; L'hydrogene

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2004-07-01

    The hydrogen as an energy system represents nowadays a main challenge (in a scientific, economical and environmental point of view). The physical and chemical characteristics of hydrogen are at first given. Then, the challenges of an hydrogen economy are explained. The different possibilities of hydrogen production are described as well as the distribution systems and the different possibilities of hydrogen storage. Several fuel cells are at last presented: PEMFC, DMFC and SOFC. (O.M.)

  19. Hydrogen Atom Collision Processes in Cool Stellar Atmospheres: Effects on Spectral Line Strengths and Measured Chemical Abundances in Old Stars

    International Nuclear Information System (INIS)

    The precise measurement of the chemical composition of stars is a fundamental problem relevant to many areas of astrophysics. State-of-the-art approaches attempt to unite accurate descriptions of microphysics, non-local thermodynamic equilibrium (non-LTE) line formation and 3D hydrodynamical model atmospheres. In this paper I review progress in understanding inelastic collisions of hydrogen atoms with other species and their influence on spectral line formation and derived abundances in stellar atmospheres. These collisions are a major source of uncertainty in non-LTE modelling of spectral lines and abundance determinations, especially for old, metal-poor stars, which are unique tracers of the early evolution of our galaxy. Full quantum scattering calculations of direct excitation processes X(nl) + H ↔ X(n'l') + H and charge transfer processes X(nl) + H ↔ X+ + H− have been done for Li, Na and Mg [1,2,3] based on detailed quantum chemical data, e.g. [4]. Rate coefficients have been calculated and applied to non-LTE modelling of spectral lines in stellar atmospheres [5,6,7,8,9]. In all cases we find that charge transfer processes from the first excited S-state are very important, and the processes affect measured abundances for Li, Na and Mg in some stars by as much as 60%. Effects vary with stellar parameters (e.g. temperature, luminosity, metal content) and so these processes are important not only for accurate absolute abundances, but also for relative abundances among dissimilar stars.

  20. Molecular structure and vibrational spectroscopic analysis of an antiplatelet drug; clopidogrel hydrogen sulphate (form 2) - A combined experimental and quantum chemical approach

    Science.gov (United States)

    Srivastava, Anubha; Mishra, Soni; Tandon, Poonam; Patel, Sarasvatkumar; Ayala, A. P.; Bansal, A. K.; Siesler, H. W.

    2010-02-01

    Clopidogrel hydrogen sulphate which belongs to a class of medicine called antiplatelet drugs. Chemically it is methyl (+)-(S)-α-(2-chlorophenyl)-4,5,6,7-tetrahydrothieno [3,2- c] pyridine-5-acetate hydrogen sulphate having the empirical formula C 16H 17ClNO 2S.HSO 4 and molecular mass 321.82 g/mol. The present study is confined to vibrational spectroscopy of the polymorph identified as form 2 of the clopidogrel hydrogen sulphate. The vibrational analysis of clopidogrel hydrogen sulphate salt (form 2) considering separately the two counterions has been performed. We also report a theoretical and experimental study of the molecular conformation and vibrational dynamics of the independent moieties of the clopidogrel hydrogen sulphate salt. The equilibrium geometry, harmonic vibrational frequencies, infrared intensities and activities of Raman scattering were calculated by ab initio Hartree-Fock and density functional theory employing B3LYP with complete relaxation in the potential energy surface using 6-311++G(d,p) basis set. The calculated wavenumbers after a proper scaling show a very good agreement with the observed values. A complete vibrational assignment is provided for the observed Raman and infrared spectra of clopidogrel hydrogen sulphate form 2.

  1. Synthesis and luminescent properties of low oxygen contained Eu2+-doped Ca-α-SiAlON phosphor from calcium cyanamide reduction

    Institute of Scientific and Technical Information of China (English)

    PIAO Xianqing; Ken-ichi Machida; Takashi Horikawa; Hiromasa Hanzawa

    2008-01-01

    A new convenient calcium cyanamide (CaCN2) reduction route was developed to synthesize the Eu2+ activated Ca-α-SiAlON phosphors containing low oxygen content. The luminescence properties of the obtained products were investigated for white LEDs application. The critical Eu2+ concentration in various hosts and its effect on the photoluminescence properties were studied. The optimized sample (10at.% Eu2+ vs. Ca2+) could be efficiently excited by the current GaN/InGaN blue LED chips and provided emission intensity competitive with that of YAG:Ce3+ (P46-Y3) standard, revealing that this phosphor was a potential candidate for phosphor-converted white LEDs.

  2. Hydrogenation of Furfural to Furfuryl Alcohol over Co-B Amorphous Catalysts Prepared by Chemical Reduction in Variable Media

    Institute of Scientific and Technical Information of China (English)

    LI, Hui; CHAI, Wei-Mei; LUO, Hong-Shan; LI, He-Xing

    2006-01-01

    Five Co-B amorphous alloy catalysts were prepared by chemical reduction in different media, including pure water and pure ethanol as well as the mixture of ethanol and water with variable ethanol content. Their catalytic properties were evaluated using liquid phase furfural hydrogenation to furfuryl alcohol as the probe reaction. It was found that the reaction media had no significant influence on either the amorphous structure of the Co-B catalyst or the electronic interaction between metallic Co and alloying B. This could successfully account for the fact that all the as-prepared Co-B catalysts exhibited almost the same selectivity to furfuryl alcohol and the same activity per surface area ( RSH ), which could be considered as the intrinsic activity, since the nature of active sites remained unchanged. However, the activity per gram of Co ( RmH ) of the as-prepared Co-B catalysts increased rapidly when the ethanol content in the water-ethanol mixture used as the reaction medium for catalyst preparation increased. This could be attributed to the rapid increase in the surface area possibly owing to the presence of more oxidized boron species which could serve as a support for dispersing the Co-B amorphous alloy particles.

  3. Performance of Ni-based, Fe-based and Co-based Oxygen Carriers in Chemical-Looping Hydrogen Generation

    Institute of Scientific and Technical Information of China (English)

    Liang Hao; Zhang Xiwen; Fang Xiangchen; Yuan Honggang

    2013-01-01

    Ni-based, Fe-based and Co-based oxygen carriers with perovskite oxides used as the supports were prepared by citric acid complexation method. The oxygen carriers were characterized by thermal analysis, H2-temperature-programmed reduction and X-ray diffraction methods. Performance tests were evaluated through Chemical-Looping Hydrogen Genera-tion in a ifxed-bed reactor operating at atmospheric pressure. The characterization results showed that all samples were composed of metal oxides and perovskite oxides. Performance results indicated that CH4 conversion over the oxygen car-riers decreased in the following order:NiO/LaNiO3>Co2O3/LaCoO3>Fe2O3/LaFeO3. The ability of NiO/LaNiO3 and Fe2O3/LaFeO3 to decompose water was stronger than that of Co2O3/LaCoO3 as evidenced by our experiments. H2 amounting to 80 mL upon reacting on methane in every cycle could be completely oxidized by NiO/LaNiO3 at 900℃in the period from the third cycle to the eighth cycle.

  4. Glassy carbon electrode modified with a graphene oxide/poly(o-phenylenediamine) composite for the chemical detection of hydrogen peroxide

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Van Hoa [School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749 (Korea, Republic of); Department of Chemistry, Nha Trang University, 2 Nguyen Dinh Chieu, Nha Trang (Viet Nam); Tran, Trung Hieu [School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749 (Korea, Republic of); Shim, Jae-Jin, E-mail: jjshim@yu.ac.kr [School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749 (Korea, Republic of)

    2014-11-01

    Conducting poly(o-phenylenediamine) (POPD)/graphene oxide (GO) composites were prepared using a facile and efficient method involving the in-situ polymerization of OPD in the presence of GO in an aqueous medium. Copper sulfate was used as an oxidative initiator for the polymerization of OPD. Scanning electron microscopy and transmission electron microscopy images showed that POPD microfibrils were formed and distributed relatively uniformly with GO sheets in the obtained composites. X-ray diffraction results revealed the highly crystal structure of POPD. This composite exhibited good catalytic activity and stability. These results highlight the potential applications of POPD/GO composites as excellent electrochemical sensors. The composites were used to modify glass carbon electrodes for the chemical detection of hydrogen peroxide in aqueous media. - Highlights: • Graphene oxide/poly(o-phenylenediamine) composites were prepared efficiently. • POPD microfibrils were distributed relatively uniformly with GO sheets. • The composite exhibited good catalytic activity and stability for H{sub 2}O{sub 2} sensing.

  5. Methane as an effective hydrogen source for single-layer graphene synthesis on Cu foil by plasma enhanced chemical vapor deposition.

    Science.gov (United States)

    Kim, Yong Seung; Lee, Jae Hong; Kim, Young Duck; Jerng, Sahng-Kyoon; Joo, Kisu; Kim, Eunho; Jung, Jongwan; Yoon, Euijoon; Park, Yun Daniel; Seo, Sunae; Chun, Seung-Hyun

    2013-02-01

    A single-layer graphene is synthesized on Cu foil in the absence of H(2) flow by plasma enhanced chemical vapor deposition (PECVD). In lieu of an explicit H(2) flow, hydrogen species are produced during the methane decomposition process into their active species (CH(xpower. The resulting grain size (the nucleation density) has a maximum (minimum) at 50 W and saturates when the plasma power is higher than 120 W because hydrogen partial pressures are effectively tuned by a simple control of the plasma power. Raman spectroscopy and transport measurements show that decomposed methane alone can provide a sufficient amount of hydrogen species for high-quality graphene synthesis by PECVD. PMID:23299508

  6. Hydrogen production by the solar-powered hybrid sulfur process: Analysis of the integration of the CSP and chemical plants in selected scenarios

    Science.gov (United States)

    Liberatore, Raffaele; Lanchi, Michela; Turchetti, Luca

    2016-05-01

    The Hybrid Sulfur (HyS) is a water splitting process for hydrogen production powered with high temperature nuclear heat and electric power; among the numerous thermo-chemical and thermo-electro-chemical cycles proposed in the literature, such cycle is considered to have a particularly high potential also if powered by renewable energy. SOL2HY2 (Solar to Hydrogen Hybrid Cycles) is a 3 year research project, co-funded by the Fuel Cells and Hydrogen Joint Undertaking (FCH JU). A significant part of the project activities are devoted to the analysis and optimization of the integration of the solar power plant with the chemical, hydrogen production plant. This work reports a part of the results obtained in such research activity. The analysis presented in this work builds on previous process simulations used to determine the energy requirements of the hydrogen production plant in terms of electric power, medium (550°C) temperature heat. For the supply of medium temperature (MT) heat, a parabolic trough CSP plant using molten salts as heat transfer and storage medium is considered. A central receiver CSP (Concentrated Solar Power) plant is considered to provide high temperature (HT) heat, which is only needed for sulfuric acid decomposition. Finally, electric power is provided by a power block included in the MT solar plant and/or drawn from the grid, depending on the scenario considered. In particular, the analysis presented here focuses on the medium temperature CSP plant, possibly combined with a power block. Different scenarios were analysed by considering plants with different combinations of geographical location and sizing criteria.

  7. A Theoretical Study of two Novel Concept Systems for Maximum Thermal-Chemical Conversion of Biomass to Hydrogen

    Directory of Open Access Journals (Sweden)

    Jacob N. Chung

    2014-01-01

    Full Text Available Two concept systems that are based on the thermochemical process of high-temperature steam gasification of lignocellulosic biomass and municipal solid waste are introduced. The primary objectives of the concept systems are 1 to develop the best scientific, engineering, and technology solutions for converting lignocellulosic biomass, as well as agricultural, forest and municipal waste to clean energy (pure hydrogen fuel, and 2 to minimize water consumption and detrimental impacts of energy production on the environment (air pollution and global warming. The production of superheated steam is by hydrogen combustion using recycled hydrogen produced in the first concept system while in the second concept system concentrated solar energy is used for the steam production. A membrane reactor that performs the hydrogen separation and water gas shift reaction is involved in both systems for producing more pure hydrogen and CO2 sequestration. Based on obtaining the maximum hydrogen production rate the hydrogen recycled ratio is around 20% for the hydrogen combustion steam heating system. Combined with pure hydrogen production, both high temperature steam gasification systems potentially possess more than 80% in first law overall system thermodynamic efficiencies.

  8. Water-Soluble Iridium-NHC-Phosphine Complexes as Catalysts for Chemical Hydrogen Batteries Based on Formate.

    Science.gov (United States)

    Horváth, Henrietta; Papp, Gábor; Szabolcsi, Roland; Kathó, Ágnes; Joó, Ferenc

    2015-09-21

    Molecular hydrogen, obtained by water electrolysis or photocatalytic water splitting, can be used to store energy obtained from intermittent sources such as wind and solar power. The storage and safe transportation of H2 , however, is an open and central question in such a hydrogen economy. Easy-to-synthesize, water-soluble iridium-N-heterocyclic carbene-phosphine (Ir(I) -NHC-phosphine) catalysts show unprecedented high catalytic activity in dehydrogenation of aqueous sodium formate. Fast reversible generation and storage of hydrogen can be achieved with these catalysts by a simple decrease or increase in the hydrogen pressure, respectively. PMID:26289830

  9. Synthesis of new structurally related cyanamide compounds LiM(CN{sub 2}){sub 2} where M is Al{sup 3+}, In{sup 3+} or Yb{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Kubus, Mariusz, E-mail: mariusz.kubus@anorg.uni-tuebingen.de [Abteilung für Festkörperchemie und Theoretische Anorganische Chemie, Institut für Anorganische Chemie, Auf der Morgenstelle 18, Universität Tübingen, 72076 Tübingen (Germany); Heinicke, Robert; Ströbele, Markus [Abteilung für Festkörperchemie und Theoretische Anorganische Chemie, Institut für Anorganische Chemie, Auf der Morgenstelle 18, Universität Tübingen, 72076 Tübingen (Germany); Enseling, David; Jüstel, Thomas [Fachhochschule Münster, Labor für Angewandte Materialwissenschaft, Stegerwaldstrasse 39, D-48565 Steinfurt (Germany); Meyer, H.-Jürgen, E-mail: juergen.meyer@uni-tuebingen.de [Abteilung für Festkörperchemie und Theoretische Anorganische Chemie, Institut für Anorganische Chemie, Auf der Morgenstelle 18, Universität Tübingen, 72076 Tübingen (Germany)

    2015-02-15

    Highlights: • New cyanamide compounds LiM(CN{sub 2}){sub 2} where M is Al{sup 3+}, In{sup 3+} or Yb{sup 3+}. • New luminescent material LiIn(CN{sub 2}){sub 2}:Tb{sup 3+}. • Reduction in efficiency of luminescence with temperature increase. - Abstract: New ternary cyanamide compounds isostructural to LiY(CN{sub 2}){sub 2} were obtained by solid state metathesis reaction. The crystal structure of LiAl(CN{sub 2}){sub 2} was determined by single crystal X-ray diffraction, the structures of LiIn(CN{sub 2}){sub 2} and LiYb(CN{sub 2}){sub 2} were solved from X-ray powder diffraction data. Photoluminescence properties of Tb{sup 3+}-doped LiIn(CN{sub 2}){sub 2} are reported too.

  10. The role of hydrogen in oxygen-assisted chemical vapor deposition growth of millimeter-sized graphene single crystals

    Science.gov (United States)

    Zhao, Pei; Cheng, Yu; Zhao, Dongchen; Yin, Kun; Zhang, Xuewei; Song, Meng; Yin, Shaoqian; Song, Yenan; Wang, Peng; Wang, Miao; Xia, Yang; Wang, Hongtao

    2016-03-01

    Involving oxygen in the traditional chemical vapor deposition (CVD) process has proven a promising approach to achieve large-scale graphene single crystals (GSCs), but its many relevant fundamental aspects are still not fully understood. Here we report a systematic study on the role of hydrogen in the growth of millimeter-sized GSCs using enclosure-like Cu structures via the oxygen-assisted CVD process. Results show that GSCs have different first layer growth behaviors on the inside and outside surfaces of a Cu enclosure when the H2 environment is varied, and these behaviors will consequently and strongly influence the adlayer formation in these GSCs, leading to two entirely different growth modes. Low H2 partial pressure (PH2) tends to result in fast growth of dendritically shaped GSCs with multiple small adlayers, but high PH2 can modify the GSC shape into hexagons with single large adlayer nuclei. This difference of adlayers is attributed to the different C diffusion paths determined by the shapes of their host GSCs. On the basis of these observations, we developed an isothermal two-step method to obtain GSCs with significantly improved growth rate and sample quality, in which low PH2 is first set to accelerate the growth rate followed by high PH2 to restrict the adlayer nuclei. Our results prove that the growth of GSCs can reach a reasonable optimization between their growth rates and sample quality by simply adjusting the CVD H2 environment, which we believe will lead to more improvements in graphene synthesis and fundamental insight into the related growth mechanisms.Involving oxygen in the traditional chemical vapor deposition (CVD) process has proven a promising approach to achieve large-scale graphene single crystals (GSCs), but its many relevant fundamental aspects are still not fully understood. Here we report a systematic study on the role of hydrogen in the growth of millimeter-sized GSCs using enclosure-like Cu structures via the oxygen-assisted CVD

  11. Insight into the effect of hydrogenation on efficiency of hydrothermal liquefaction and physico-chemical properties of biocrude oil.

    Science.gov (United States)

    Li, HongYi; Hu, Jiao; Zhang, ZhiJian; Wang, Hang; Ping, Fan; Zheng, ChangFeng; Zhang, HaiLuo; He, Qiang

    2014-07-01

    Hydrothermal liquefaction of Nannochloropsis salina (N. salina) and larvae-vermicompost were conducted under both non-hydrogenating and hydrogenating subcritical conditions using H2 and Ni-Mo/Al2O3. Hydrogenation raised biocrude yields from 33.2% to 43.5% (vermicompost) and 55.6% to 78.5% (N. salina), whereas high heat values increased from 32.89 to 34.24 MJ/kg (vermicompost) and 36.30 to 37.53 MJ/kg (N. salina). Compared with the non-hydrogenated HTL process, the contents of acids, amides, phenols, and alcohols decreased, whereas hydrocarbons content increased. More branched cyclic nitrogenous compounds were detected in the hydrogenated biocrudes, whereas the aromatic/hetero-aromatic functionality was somewhat decreased. Smaller molecular weights and polydispersity index of the hydrogenated biocrudes were also detected. Results show that hydrogenation enhanced the removal of hydrophilic functional groups and the stabilization of radicals, thereby leading to the inhibition of loss of mass toward liquid and gaseous products and the upgrading of oil quality. PMID:24813386

  12. Mineralogical and chemical investigations of abiotic hydrogen development in incinerator residues; Mineralogische und chemische Untersuchungen zur abiotischen Wasserstoffentwicklung in Muellverbrennungsrueckstaenden

    Energy Technology Data Exchange (ETDEWEB)

    Magel, G.

    2003-07-01

    The monofill of Waldering is the oldest monofill in Bavaria for residues of a municipal solid waste incinerator (MSWI). Bottom ash (BA) and residues of the air pollution control system (APC) from the MSWI in Rosenheim have been deposited since 1976. After the first section was entirely filled, it was covered with a landfill liner and cap, according to the German law for waste treatment. During final operations on the landfill liner a deflagration occurred. The analysis of the landfill gas revealed that hydrogen gas was produced within the landfill body. Due to the sealing, the hydrogen gas could not diffuse to the atmosphere but concentrates within the landfill. Above a concentration of 4%, hydrogen is an explosive gas in the presence of oxygen. Abiotic hydrogen generation in MSWI-residues has been noted in only a few studies which conclude that hydrogen production largely terminates after three months and therefore can be neglected in the long range. However, the occurrence of the long-term hydrogen production in Waldering contradicts these statements. Landfill gas from another landfill for MSWI-residues, situated in Franklin, New Hampshire (USA), contains 5.1% hydrogen. Therefore hydrogen production in a monofill is not unique to Waldering. Deposited material from both monofills has been analysed and compared to fresh material. Owing to different methods of deposition, the BA and APC-residues of the monofill of Waldering were investigated separately whereas composite samples of BA and APC-residues were analysed from the monofill of Franklin. The experimental data of this study - in agreement with some literature studies - show that the production of hydrogen in MSWI-residues is due to hydration reactions of non-noble metals, especially aluminium. (orig.)

  13. Investigating the Chemical Reactivity for Hydrogen in Siliciclastic Sediments: two Work Packages of the H2STORE Project

    Science.gov (United States)

    De Lucia, M.; Pilz, P.

    2014-12-01

    The H2STORE ("Hydrogen to Store") collaborative project, funded by the German government, investigates the feasibility of industrial-scale hydrogen storage from excess wind energy in siliciclastic depleted gas and oil reservoirs or suitable saline aquifers. In particular, two work packages (geochemical experiments and modelling) hosted at the German Research Centre for Geosciences (GFZ) focus on the possible impact of hydrogen on formation fluids and on the mineralogical, geochemical and petrophysical properties of reservoirs and caprocks. Laboratory experiments expose core samples from several potential reservoirs to pure hydrogen or hydrogen mixtures under site-specific conditions (temperatures up to 200 °C and pressure up to 300 bar). The resulting qualitative and, whereas possible, quantitative data are expected to ameliorate the precision of predictive geochemical and reactive transport modelling, which is also performed within the project. The combination of experiments and models will improve the knowledge about: (1) solubility model and mixing rule for of hydrogen and its gas mixtures in high saline formation fluids; (2) hydrogen reactivity in a broad spectrum of P-T conditions; (3) thermodynamics and kinetics of mineral dissolution or precipitation reactions and redox processes. It is known that under specific P-T conditions reactions between hydrogen and anorganic rock components such as carbonates can occur. However these conditions have never been precisely defined to date. A precise estimation of the hydrogen impact on reservoir behavior of different siliciclastic rock types is crucial for site selection and optimization of storage depth. Enhancing the overall understanding of such systems will benefit the operational reliability, the ecological tolerance, and the economic efficiency of future energy storing plants, crucial aspects for public acceptance and for industrial investors.

  14. Physical, chemical and microbiological properties of mixed hydrogenated palm kernel oil and cold-pressed rice bran oil as ingredients in non-dairy creamer

    Directory of Open Access Journals (Sweden)

    Kunakorn Katsri

    2014-02-01

    Full Text Available The physical, chemical and microbiological properties of hydrogenated palm kernel oil (PKO and cold-pressed rice bran oil (RBOas ingredients in the production of liquid and powdered non-dairy creamer (coffee whitener were studied. The mixing ratios between hydrogenated PKO and cold-pressed RBO were statistically designed as of 100:0, 90:10,80:20, 70:30, 60:40, 50:50, 40:60, 30:70, 20:80, 10:90 and 0:100.The color, absorbanceand viscosity of the mixtures were investigated. As the ratio of cold-pressed RBO increased, the color became darker (L*of 93.06 to 86.25 and the absorbance significantly increased, while the viscosity of the mixtures of 20:80, 10:90 and 0:100 (54 cp. were the highest amongst the ratios tested.The hydrogenated PKO and cold-pressed RBO mixtures were further chemically tested for fatty acids, -oryzanol, -tocopherol, trans-fat contents andantioxidant activity. There were 10 fatty acids present in hydrogenated PKO with saturated fatty acid being the most predominant. Comparatively, there were only 5 fatty acids found in cold-pressed RBO with monounsaturated fatty acid being the major fatty acid. -Oryzanol and -tocopherol contents were higher with increasingcold-pressed RBO from 0-100% (0 to 1,155.00 mg/100g oil and 0.09 to 30.82 mg/100g oil, respectively. Antioxidant activity was increased with increasing cold-pressed RBO from 0-100% (9.26 to 94.24%.The pure hydrogenated PKO contained higher trans-fat content than that of the 90:10 and 80:20 mixtures (2.73, 1.93 and 1.85mg/100g oil,respectively while other samples had no trans-fat. No microorganisms were present in any of the samples.Therefore, substitution of hydrogenated PKO by cold-pressed RBO from 30-100% would offer more nutritional values and better chemical and physical properties of non-dairy creamer.

  15. Effect of calcium cyanamid synthetic drug on Schistosoma japonicum egg morphology%氰氨化钙合成药物对血吸虫虫卵形态学影响

    Institute of Scientific and Technical Information of China (English)

    周义生; 彭国华; 胡主花; 冯小武; 朱蓉; 魏望远; 郭家钢

    2015-01-01

    目的:观察虫卵经氰氨化钙合成药物作用后的形态改变,为进一步研究氰氨化钙合成药物杀灭血吸虫虫卵作用机理提供依据。方法向含有血吸虫虫卵的阳性牛粪中加入氰氨化钙合成药物并搅拌,模拟野粪自然形态堆放于洲滩上;同时设空白对照。于1、2、3、7d后分别取样,收集血吸虫虫卵,于显微镜下观察虫卵形态。结果虫卵经氰氨化钙合成药物作用后,颜色逐步加深,毛蚴萎缩,卵壳变厚,3d后胚膜不完整,7d后毛蚴严重变形;对照组毛蚴未见明显萎缩。结论氰氨化钙合成药物对虫卵胚膜及毛蚴有损伤作用,且随时间延长而损伤加重。%Objective To study the morphological change of Schistosoma japonicum eggs processed by calcium cyanamide synthetic drug,so as to provide the basis for further study of the mechanism that calcium cyanamide synthetic drug to schisto⁃some eggs. Methods The calcium cyanamide synthetic drug was added to the cattle feces containing schistosome eggs and mixed up,and then the cattle feces was stacked as original shape on the marshland. Blank controls were set at the same time. The cattle feces samples were collected and the schistosome eggs were observed under a microscope on the 1st,2nd,3rd,7th day after the experiment. Results By the effect of calcium cyanamide synthetic drug,the color of eggs was deepening gradual⁃ly,the miracidia were atrophied,and the shells of eggs were thickened. The embryonic membrane of miracidia was no longer completed 3 days later,and the miracidia were deformed severely 7 days later. The atrophy of miracidia was not obvious in the blank controls. Conclusion The schistosome miracidia and embryonic membrane can be damaged by the calcium cyanamide synthetic drug,and worse damaged with time extending.

  16. Evaluating the safety and regulatory aspects of the combined nuclear/chemical complex for Hydrogen production / Gerhardus Petrus Schalkwyk

    OpenAIRE

    Schalkwyk, Gerhardus Petrus

    2008-01-01

    Recently there has been an exceptional resurgence of interest in the nuclear power industry and the cogeneration of hydrogen from nuclear process heat and electricity, with climate change and energy security the main drivers for the implementation of these technologies. Nuclear-assisted hydrogen production technologies include electrochemical, thermochemical and hybrid-thermochemical options that respectively require electricity, high-temperature process heat and both electricity and high-tem...

  17. Role of atomic hydrogen density and energy in low power chemical vapor deposition synthesis of diamond films

    International Nuclear Information System (INIS)

    Polycrystalline diamond films were synthesized on silicon substrates without diamond seeding by a very low power (∼40-80 W) microwave plasma continuous vapor deposition reaction of a mixture of helium-hydrogen-methane (48.2/48.2/3.6%) or argon-hydrogen-methane (17.5/80/2.5%). However, predominantly graphitic carbon films or no films formed when neon, krypton, or xenon was substituted for helium or argon. The films were characterized by time of flight secondary ion mass spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, scanning electron microscopy, and X-ray diffraction. It is proposed that each of He+ and Ar+ served as a catalyst with atomic hydrogen to form an energetic plasma since only plasmas having these ions in the presence of atomic hydrogen showed significantly broadened H α lines corresponding to an average hydrogen atom temperature of >100 eV as reported previously. It was found that not only the energy, but also the H density uniquely increases in He-H2 and Ar-H2 plasmas. Bombardment of the carbon surface by highly energetic hydrogen formed by the catalysis reaction may play a role in the formation of diamond. Then, by this novel pathway, the relevance of the CO tie line is eliminated along with other stringent conditions and complicated and inefficient techniques which limit broad application of the versatility and superiority of diamond thin film technology

  18. Hydrogen Production From Water By Thermo-Chemical Methods (UT-3): Evaluation of Side Reactions By Simulation Process

    International Nuclear Information System (INIS)

    Hydogen fuel with its advantages will be able to replace all the positions of fossil fuels post oil and gas or migas. Among the advantages of hydrogen fuel are pollution free, abundant of raw material in the form of water molecule, flexible in application, able to stroge and transport as well as fossil energy sources (oil and gas). Hydogen could be produced from water by means of thermochemical, thermolysis, photolysis and electrolysis. Nuclear heat (HTGR), solar heat or waste heat from steel industry can be used as energy source for these processes. In case of thermochemical method, some problems realated to production process should be studied and evaluated. Simulation is considered can be applied to study the effects of side reactions and also to resolve its problems in hydrogen production process. In this paper is reported the evalution results of hydrogen production process by thermochemical (UT-3) through both of the experimental and computer simulation. It has been proposed a new flow chart of hydrogen production to achieve the hydrogen production continuously. A simulator has been developed based on experimental data and related mathematical equations. This simulator can be used to scle-up the UT-3 thermochemical cycle for hydrogen production process

  19. Growth of graphene on Cu foils by microwave plasma chemical vapor deposition: The effect of in-situ hydrogen plasma post-treatment

    Science.gov (United States)

    Fang, Liping; Yuan, Wen; Wang, Bing; Xiong, Ying

    2016-10-01

    Microwave plasma chemical vapor deposition (MPCVD) is a promising method for the large-scale production of high-quality graphene. The aim of this work is to investigate the effect of in-situ hydrogen plasma post-treatment on the MPCVD-grown graphene films. By simply varying the duration time of in-situ hydrogen plasma, surface morphology, number of layers and defect density of as-grown graphene films can be manipulated. The role of hydrogen plasma can be proposed from our observations, promoting to further grow graphene films in the early stage and consequently acting as an etching agent to thin graphene films in the later stage. On the basis of above mechanism, monolayer graphene films with low defect density and smooth surface can be grown by adjusting the times of the growing step and the plasma post-treatment step. This additional in-situ hydrogen plasma post-treatment may be significant for growing well-defined graphene films with controllable defects and number of layers.

  20. Hydrogen production by ethanol partial oxidation over nano-iron oxide catalysts produced by chemical vapour synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Ahmed, Wael Ahmed Abou Taleb Sayed

    2011-01-13

    This work presents the experimental results of the synthesis of unsupported and supported SiC iron oxide nanoparticles and their catalytic activity towards ethanol partial oxidation. For comparison, further unsupported iron oxide phases were investigated towards the ethanol partial oxidation. These {gamma}-Fe{sub 2}O{sub 3} and {alpha}/{gamma}-Fe{sub 2}O{sub 3} phase catalysts were prepared by the CVS method using Fe(CO){sub 5} as precursor, supplied by another author. The {alpha}-Fe{sub 2}O{sub 3} and SiC nanoparticles were prepared by the CVS method using a home made hot wall reactor technique at atmospheric pressure. Ferrocene and tetramethylsilane were used as precursor for the production process. Process parameters of precursor evaporation temperature, precursor concentration, gas mixture velocity and gas mixture dilution were investigated and optimised to produce particle sizes in a range of 10 nm. For Fe{sub 2}O{sub 3}/SiC catalyst series production, a new hot wall reactor setup was used. The particles were produced by simultaneous thermal decomposition of ferrocene and tetramethylsilane in one reactor from both sides. The production parameters of inlet tube distance inside the reactor, precursor evaporation temperature and carrier gas flow were investigated to produce a series of samples with different iron oxide content. The prepared catalysts composition, physical and chemical properties were characterized by XRD, EDX, SEM, BET surface area, FTIR, XPS and dynamic light scattering (DLS) techniques. The catalytic activity for the ethanol gas-phase oxidation was investigated in a temperature range from 260 C to 290 C. The product distributions obtained over all catalysts were analysed with mass spectrometry analysis tool. The activity of bulk Fe{sub 2}O{sub 3} and SiC nanoparticles was compared with prepared nano-iron oxide phase catalysts. The reaction parameters, such as reaction temperature and O{sub 2}/ethanol ratio were investigated. The catalysts

  1. Response Behaviour of a Hydrogen Sensor Based on IonicConducting Polymer-metal Interfaces Prepared by the ChemicalReduction Method

    Directory of Open Access Journals (Sweden)

    Werner Weppner

    2006-04-01

    Full Text Available A solid-state amperometric hydrogen sensor based on a protonated Nafionmembrane and catalytic active electrode operating at room temperature was fabricated andtested. Ionic conducting polymer-metal electrode interfaces were prepared chemically byusing the impregnation-reduction method. The polymer membrane was impregnated withtetra-ammine platinum chloride hydrate and the metal ions were subsequently reduced byusing either sodium tetrahydroborate or potassium tetrahydroborate. The hydrogen sensingcharacteristics with air as reference gas is reported. The sensors were capable of detectinghydrogen concentrations from 10 ppm to 10% in nitrogen. The response time was in therange of 10-30 s and a stable linear current output was observed. The thin Pt films werecharacterized by XRD, Infrared Spectroscopy, Optical Microscopy, Atomic ForceMicroscopy, Scanning Electron Microscopy and EDAX.

  2. Screening of NiFe2O4 Nanoparticles as Oxygen Carrier in Chemical Looping Hydrogen Production

    DEFF Research Database (Denmark)

    Liu, Shuai; He, Fang; Huang, Zhen;

    2016-01-01

    ) porosity test. The performance of the prepared materials was first evaluated in a TGA reactor through a CO reduction and subsequent steam oxidation process. Then a complete redox process was conducted in a fixed-bed reactor, where the NiFe2O4 oxygen carrier was first reduced by simulated biomass pyrolysis...... gas (24% H2 + 24% CO + 12% CO2 + N2 balance), then reacted with steam to produce H2, and finally fully oxidized by air. The NiFe2O4 oxygen carrier prepared by the sol gel method showed the best capacity for hydrogen production and the highest recovery degree of lattice oxygen, in agreement with the......The objective of this paper is to systematically investigate the influences of different preparation methods on the properties of NiFe2O4 nanoparticles as oxygen carrier in chemical looping hydrogen production (CLH). The solid state (SS), coprecipitation (CP), hydrothermal (HT), and sol-gel (SG...

  3. Gas doping ratio effects on p-type hydrogenated nanocrystalline silicon thin films grown by hot-wire chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Luo, P.Q. [Solar Energy Institute, Department of Physics, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China)], E-mail: robt@sjtu.edu.cn; Zhou, Z.B. [Solar Energy Institute, Department of Physics, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China)], E-mail: zbzhou@sjtu.edu.cn; Chan, K.Y. [Thin Film Laboratory, Faculty of Engineering, Multimedia University, Jalan Multimedia, Cyberjaya 63100, Selangor (Malaysia); Tang, D.Y.; Cui, R.Q.; Dou, X.M. [Solar Energy Institute, Department of Physics, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China)

    2008-12-30

    Hydrogenated nanocrystalline silicon (nc-Si:H) grown by hot-wire chemical vapor deposition (HWCVD) has recently drawn significant attention in the area of thin-film large area optoelectronics due to possibility of high deposition rate. We report on the effects of diborane (B{sub 2}H{sub 6}) doping ratio on the microstructural and optoelectrical properties of the p-type nc-Si:H thin films grown by HWCVD at low substrate temperature of 200 deg. C and with high hydrogen dilution ratio of 98.8%. An attempt has been made to elucidate the boron doping mechanism of the p-type nc-Si:H thin films deposited by HWCVD and the correlation between the B{sub 2}H{sub 6} doping ratio, crystalline volume fraction, optical band gap and dark conductivity.

  4. The role of boron nitride nanotube as a new chemical sensor and potential reservoir for hydrogen halides environmental pollutants

    Science.gov (United States)

    Yoosefian, Mehdi; Etminan, Nazanin; Moghani, Maryam Zeraati; Mirzaei, Samaneh; Abbasi, Shima

    2016-10-01

    Density functional theory (DFT) studies on the interaction of hydrogen halides (HX) environmental pollutants and the boron nitride nanotubes (BNNTs) have been reported. To exploit the possibility of BNNTs as gas sensors, the adsorption of hydrogen fluoride (HF), hydrogen chloride (HCl) and hydrogen bromide (HBr) on the side wall of armchair (5,5) boron nitride nanotubes have been investigated. B3LYP/6-31G (d) level were used to analyze the structural and electronic properties of investigate sensor. The adsorption process were interpreted by highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO), quantum theory of atoms in molecules (QTAIM), natural bond orbital (NBO) and molecular electrostatic potential (MEP) analysis. Topological parameters of bond critical points have been used to calculate as measure of hydrogen bond (HB) strength. Stronger binding energy, larger charge transfer and charge density illustrate that HF gas possesses chemisorbed adsorption process. The obtained results also show the strongest HB in HF/BNNT complex. We expect that results could provide helpful information for the design of new BNNTs based sensing devices.

  5. Best mix of primary energy resources by renewable energy and fossil fuel with CCS in view of security,stability and sustainability——A vision on hydrogen supply chain by organic chemical hydride method

    Institute of Scientific and Technical Information of China (English)

    Junichi; SAKAGUCHI

    2010-01-01

    The best mix scenario by renewable energy and fossil fuel with or without CCS(Carbon Dioxide Capture and Storage) would be a solution to compromise Greenhouse Gases emission issue caused by carbon dioxide(CO2),and depletion of crude oil and natural gas reserves.As fossil fuel with pre-combustion CCS means hydrogen manufacturing and also hydrogen can be produced via electrolysis with renewable energy,it is desirable to establish transportation and storage systems of hydrogen as a clean energy.In this paper a vision on Hydrogen Supply Chain by Organic Chemical Hydride(OCH) Method as well as comparison of CCS configuration are discussed.

  6. CHEMICALS

    CERN Multimedia

    Medical Service

    2002-01-01

    It is reminded that all persons who use chemicals must inform CERN's Chemistry Service (TIS-GS-GC) and the CERN Medical Service (TIS-ME). Information concerning their toxicity or other hazards as well as the necessary individual and collective protection measures will be provided by these two services. Users must be in possession of a material safety data sheet (MSDS) for each chemical used. These can be obtained by one of several means : the manufacturer of the chemical (legally obliged to supply an MSDS for each chemical delivered) ; CERN's Chemistry Service of the General Safety Group of TIS ; for chemicals and gases available in the CERN Stores the MSDS has been made available via EDH either in pdf format or else via a link to the supplier's web site. Training courses in chemical safety are available for registration via HR-TD. CERN Medical Service : TIS-ME :73186 or service.medical@cern.ch Chemistry Service : TIS-GS-GC : 78546

  7. Miniaturized and green method for determination of chemical oxygen demand using UV-induced oxidation with hydrogen peroxide and single drop microextraction

    International Nuclear Information System (INIS)

    We report on a green method for the determination of low levels of chemical oxygen demand. It is based on the combination of (a) UV-induced oxidation with hydrogen peroxide, (b) headspace single-drop microextraction with in-drop precipitation, and (c) micro-turbidimetry. The generation of CO2 after photolytic oxidation followed by its sequestration onto a microdrop of barium hydroxide gives rise to a precipitate of barium carbonate which is quantified by turbidimetry. UV-light induced oxidation was studied in the absence and presence of H2O2, ultrasound, and ferrous ion. Determinations of chemical oxygen demand were performed using potassium hydrogen phthalate as a model compound. The optimized method gives a calibration curve that is linear between 3.4 and 20 mg L−1 oxygen. The detection limit was 1.2 mg L−1 of oxygen, and the repeatability (as relative standard deviation) was around 5 %. The method was successfully applied to the determination of chemical oxygen demand in different natural waters and a synthetic wastewater. (author)

  8. Evidence for excited-state intramolecular proton transfer in 4-chlorosalicylic acid from combined experimental and computational studies: Quantum chemical treatment of the intramolecular hydrogen bonding interaction

    Energy Technology Data Exchange (ETDEWEB)

    Paul, Bijan Kumar [Department of Chemistry, University of Calcutta, 92 Acharya Prafulla Chandra Road, Calcutta 700009 (India); Guchhait, Nikhil, E-mail: nikhil.guchhait@rediffmail.com [Department of Chemistry, University of Calcutta, 92 Acharya Prafulla Chandra Road, Calcutta 700009 (India)

    2012-07-25

    Highlights: Black-Right-Pointing-Pointer Experimental and computational studies on the photophysics of 4-chlorosalicylic acid. Black-Right-Pointing-Pointer Spectroscopically established ESIPT reaction substantiated by theoretical calculation. Black-Right-Pointing-Pointer Quantum chemical treatment of IMHB unveils strength, nature and directional nature. Black-Right-Pointing-Pointer Superiority of quantum chemical treatment of H-bond over geometric criteria. Black-Right-Pointing-Pointer Role of H-bond as a modulator of aromaticity. -- Abstract: The photophysical study of a pharmaceutically important chlorine substituted derivative of salicylic acid viz., 4-chlorosalicylic acid (4ClSA) has been carried out by steady-state absorption, emission and time-resolved emission spectroscopy. A large Stokes shifted emission band with negligible solvent polarity dependence marks the spectroscopic signature of excited-state intramolecular proton transfer (ESIPT) reaction in 4ClSA. Theoretical calculation by ab initio and Density Functional Theory methods yields results consistent with experimental findings. Theoretical potential energy surfaces predict the occurrence of proton transfer in S{sub 1}-state. Geometrical and energetic criteria, Atoms-In-Molecule topological parameters, Natural Bond Orbital population analysis have been exploited to evaluate the intramolecular hydrogen bond (IMHB) interaction and to explore its directional nature. The inter-correlation between aromaticity and resonance assisted H-bond is also discussed in this context. Our results unveil that the quantum chemical treatment is a more accurate tool to assess hydrogen bonding interaction in comparison to geometrical criteria.

  9. Effects of H{sub 2} and Ar flow rates on the deposition of hydrogenated silicon thin films by an inductive coupled plasma-chemical vapor deposition system

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chuan, E-mail: cli10@yahoo.com [Department of Biomedical Engineering, National Yang Ming University, Taipei, 11221, Taiwan (China); Department of Mechanical Engineering, National Central University, Jhongli, Taoyuan, 32001, Taiwan (China); Hsieh, J.H. [Department of Materials Engineering, Ming Chi University of Technology, Taishan, Taipei, 24301, Taiwan (China); Huang, K.L.; Shao, Yu Ting; Chen, Yi Wen [Department of Biomedical Engineering, National Yang Ming University, Taipei, 11221, Taiwan (China)

    2013-10-01

    Amorphous hydrogenated silicon films were deposited on quartz substrates in an inductive coupled plasma-chemical vapor deposition system with four internal low inductance antennas units. Different Ar and hydrogen flow rates were tested for their influences on the structures of deposited films. For monitoring purposes, Langmuir probe and optical emission spectrometer were installed to detect the variation of electrical field in plasma during deposition. Data from Langmuir probe and optical emission spectrometer were analyzed subsequently. After deposition, the films were examined by X-ray diffraction and Raman spectrometer for their microstructures. Results indicate that under the supply of pure Ar flow, the deposition rate can be expedited to 3.5 nm/s and amorphous films were formed on quartz substrates. With the supply of mixed hydrogen and argon (Ar 15 sccm + H{sub 2} 50 sccm + SiH{sub 4} 50 sccm), the deposition rate can reach 4.5 nm/s. Although it is well known that a high supply of H{sub 2} helps the formation of micro-crystalline silicon, these deposited hydrogenated Si films, confirmed by X-ray diffraction patterns and Raman spectroscopy, all maintained their amorphousness under various range of Ar and H{sub 2} flow rates. - Highlights: • Amorphous hydrogenated silicon films were deposited by inductive coupled plasma. • Different Ar and H{sub 2} flow rates were tested for their effects on the structures of films. • Under pure Ar flow, the deposition rate of can be expedited to 3.5 nm/sec. • The deposition rate reached 4.5 nm/sec under Ar 15 sccm, H{sub 2} 50 sccm, SiH{sub 4} 50 sccm. • All films are amorphous confirmed by X-ray diffraction and Raman spectroscopy.

  10. Effects of cyanamide fertilizer on microbial community structure of continuous cropping soil%氰胺类肥料对连作土壤微生物种群结构的影响

    Institute of Scientific and Technical Information of China (English)

    马军伟; 孙万春; 胡庆发; 俞巧钢; 王强; 符建荣

    2013-01-01

    structure and increasing bio‐diversity , was an effective method to overcome continuous cropping obstacles . Calcium cyanamide and dicyandiamide ( DCD) were cyanamide fertilizers , which had significant inhibition effect on harmful organisms , especially on pathogenic fungi in soil . However , effects of cyanamide fertilizers on microbial community structure and bio‐diversity of continuous cropping soil were unclear . The aim of this research was to study the effects of calcium cyanamide and dicyandiamide application on microbial community structure in continuous vegetable cropping soil . Results of the study might reveal the soil micro‐ecological mechanism of calcium cyanamide and dicyandiamide to control eggplant verticillium wilt , and provide theoretical foundation and technical guidance for cyanamide fertilizers application in agricultural production . The experimental soil was silt paddy soil and was collected from farmland in Quzhou , Zhejiang Province . In the farmland , the planting years of eggplant were more than four years , and verticillium wilt of eggplant was severe and out of control in the last year . Six treatments were designed in experiments: 1) control , 2) dicyandiamide , 3) calcium cyanamide (lime nitrogen) , 4) straw , 5) dicyandiamide + straw , 6) calcium cyanamide + straw . Soils of different treatments were incubated at 25 ℃ . Through conventional artificial culture method , quantities of bacteria , fungi and actinomycetes were recorded . Community structure and bio‐diversity of bacteria and fungi were analyzed by PCR‐DGGE . Results showed that , calcium cyanamide application effectively increased the number of bacteria , decreased the amount of fungi , improved the ratio of bacteria to fungi and actinomycetes to fungi in the continuous cropping soil . But dicyandiamide showed no distinct influence on the number of bacteria . Dicyandiamide and dicyandiamide plus rice straw application increased the ratio of bacteria to fungi with the

  11. A quantum-chemical validation about the formation of hydrogen bonds and secondary interactions in intermolecular heterocyclic systems

    Directory of Open Access Journals (Sweden)

    Boaz Galdino Oliveira

    2009-08-01

    Full Text Available We have performed a detailed theoretical study in order to understand the charge density topology of the C2H4O···C2H2 and C2H4S···C2H2 heterocyclic hydrogen-bonded complexes. Through the calculations derived from Quantum Theory of Atoms in Molecules (QTAIM, it was observed the formation of hydrogen bonds and secondary interactions. Such analysis was performed through the determination of optimized geometries at B3LYP/6-31G(d,p level of theory, by which is that QTAIM topological operators were computed, such as the electronic density ρ(r, Laplacian Ñ2ρ(r, and ellipticity ε. The examination of the hydrogen bonds has been performed through the measurement of ρ(r, Ñ2ρ(r and ε between (O···H—C and (S···H—C, whereas the secondary interaction between axial hydrogen atoms Hα and carbon of acetylene. In this insight, it was verified the existence of secondary interaction only in C2H4S···C2H2 complex because its structure is propitious to form multiple interactions.

  12. Deciphering the "chemical" nature of the exotic isotopes of Hydrogen by the MC-QTAIM analysis: Positive Muon and Muonic Helium as new members of The Periodic Table

    CERN Document Server

    Goli, Mohammad

    2013-01-01

    This report is a primarily survey on the chemical nature of the positively charged muon and muonic Helium (negatively charged muon plus Helium nucleus), as exotic isotopes of hydrogen, using the newly developed multi-component quantum theory of atoms in molecules (MC-QTAIM) analysis. To perform the analysis, the non-Born-Oppenhiemer (non-BO) ab initio methodology termed the fully variational multi-component molecular orbital method (FV-MC_MO) is used to deduce non-BO wavefunctions of various three and four-component molecular systems, as isotopomers of the orthodox hydrogen molecule, replacing proton(s) with muon, deuterium, tritium and muonic Helium. The derived three-component non-BO wavefunctions then are used for the "atoms in molecules" analysis within the context of the MC-QTAIM framework. Using various asymmetric isotopomers of hydrogen molecule, it is demonstrated that both the positively charged muon and muonic Helium are capable to form atoms in molecules in the considered molecules; thus, they reta...

  13. The Different Sensitive Behaviors of a Hydrogen-Bond Acidic Polymer-Coated SAW Sensor for Chemical Warfare Agents and Their Simulants

    Directory of Open Access Journals (Sweden)

    Yin Long

    2015-07-01

    Full Text Available A linear hydrogen-bond acidic (HBA linear functionalized polymer (PLF, was deposited onto a bare surface acoustic wave (SAW device to fabricate a chemical sensor. Real-time responses of the sensor to a series of compounds including sarin (GB, dimethyl methylphosphonate (DMMP, mustard gas (HD, chloroethyl ethyl sulphide (2-CEES, 1,5-dichloropentane (DCP and some organic solvents were studied. The results show that the sensor is highly sensitive to GB and DMMP, and has low sensitivity to HD and DCP, as expected. However, the sensor possesses an unexpected high sensitivity toward 2-CEES. This good sensing performance can’t be solely or mainly attributed to the dipole-dipole interaction since the sensor is not sensitive to some high polarity solvents. We believe the lone pair electrons around the sulphur atom of 2-CEES provide an electron-rich site, which facilitates the formation of hydrogen bonding between PLF and 2-CEES. On the contrary, the electron cloud on the sulphur atom of the HD molecule is offset or depleted by its two neighbouring strong electron-withdrawing groups, hence, hydrogen bonding can hardly be formed.

  14. Implementation of flowsheet change to minimize hydrogen and ammonia generation during chemical processing of high level waste in the defense waste processing facility

    Energy Technology Data Exchange (ETDEWEB)

    Lambert, Dan P. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Woodham, Wesley H. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Williams, Matthew S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Newell, J. David [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Luther, Michelle C. [Auburn Univ., AL (United States); Brandenburg, Clayton H. [Univ.of South Carolina, Columbia, SC (United States)

    2016-09-27

    Testing was completed to develop a chemical processing flowsheet for the Defense Waste Processing Facility (DWPF), designed to vitrify and stabilize high level radioactive waste. DWPF processing uses a reducing acid (formic acid) and an oxidizing acid (nitric acid) to rheologically thin the slurry and complete the necessary acid base and reduction reactions (primarily mercury and manganese). Formic acid reduces mercuric oxide to elemental mercury, allowing the mercury to be removed during the boiling phase of processing through steam stripping. In runs with active catalysts, formic acid can decompose to hydrogen and nitrate can be reduced to ammonia, both flammable gases, due to rhodium and ruthenium catalysis. Replacement of formic acid with glycolic acid eliminates the generation of rhodium- and ruthenium-catalyzed hydrogen and ammonia. In addition, mercury reduction is still effective with glycolic acid. Hydrogen, ammonia and mercury are discussed in the body of the report. Ten abbreviated tests were completed to develop the operating window for implementation of the flowsheet and determine the impact of changes in acid stoichiometry and the blend of nitric and glycolic acid as it impacts various processing variables over a wide processing region. Three full-length 4-L lab-scale simulations demonstrated the viability of the flowsheet under planned operating conditions. The flowsheet is planned for implementation in early 2017.

  15. Chemical, mineralogical and molecular biological characterization of the rocks and fluids from a natural gas storage deep reservoir as a baseline for the effects of geological hydrogen storage

    Science.gov (United States)

    Morozova, Daria; Kasina, Monika; Weigt, Jennifer; Merten, Dirk; Pudlo, Dieter; Würdemann, Hilke

    2014-05-01

    Planned transition to renewable energy production from nuclear and CO2-emitting power generation brings the necessity for large scale energy storage capacities. One possibility to store excessive energy produced is to transfer it to chemical forms like hydrogen which can be subsequently injected and stored in subsurface porous rock formations like depleted gas reservoirs and presently used gas storage sites. In order to investigate the feasibility of the hydrogen storage in the subsurface, the collaborative project H2STORE ("hydrogen to store") was initiated. In the scope of this project, potential reactions between microorganism, fluids and rocks induced by hydrogen injection are studied. For the long-term experiments, fluids of natural gas storage are incubated together with rock cores in the high pressure vessels under 40 bar pressure and 40° C temperature with an atmosphere containing 5.8% He as a tracer gas, 3.9% H2 and 90.3% N2. The reservoir is located at a depth of about 2 000 m, and is characterized by a salinity of 88.9 g l-1 NaCl and a temperature of 80° C and therefore represents an extreme environment for microbial life. First geochemical analyses showed a relatively high TOC content of the fluids (about 120 mg l-1) that were also rich in sodium, potassium, calcium, magnesium and iron. Remarkable amounts of heavy metals like zinc and strontium were also detected. XRD analyses of the reservoir sandstones revealed the major components: quartz, plagioclase, K-feldspar, anhydrite and analcime. The sandstones were intercalated by mudstones, consisting of quartz, plagioclase, K-feldspar, analcime, chlorite, mica and carbonates. Genetic profiling of amplified 16S rRNA genes was applied to characterize the microbial community composition by PCR-SSCP (PCR-Single-Strand-Conformation Polymorphism) and DGGE (Denaturing Gradient Gel Electrophoresis). First results indicate the presence of microorganisms belonging to the phylotypes alfa-, beta- and gamma

  16. Converting Chemical Energy to Electricity through a Three-Jaw Mini-Generator Driven by the Decomposition of Hydrogen Peroxide.

    Science.gov (United States)

    Xiao, Meng; Wang, Lei; Ji, Fanqin; Shi, Feng

    2016-05-11

    Energy conversion from a mechanical form to electricity is one of the most important research advancements to come from the horizontal locomotion of small objects. Until now, the Marangoni effect has been the only propulsion method to produce the horizontal locomotion to induce an electromotive force, which is limited to a short duration because of the specific property of surfactants. To solve this issue, in this article we utilized the decomposition of hydrogen peroxide to provide the propulsion for a sustainable energy conversion from a mechanical form to electricity. We fabricated a mini-generator consisting of three parts: a superhydrophobic rotator with three jaws, three motors to produce a jet of oxygen bubbles to propel the rotation of the rotator, and three magnets integrated into the upper surface of the rotator to produce the magnet flux. Once the mini-generator was placed on the solution surface, the motor catalyzed the decomposition of hydrogen peroxide. This generated a large amount of oxygen bubbles that caused the generator and integrated magnets to rotate at the air/water interface. Thus, the magnets passed under the coil area and induced a change in the magnet flux, thus generating electromotive forces. We also investigated experimental factors, that is, the concentration of hydrogen peroxide and the turns of the solenoid coil, and found that the mini-generator gave the highest output in a hydrogen peroxide solution with a concentration of 10 wt % and under a coil with 9000 turns. Through combining the stable superhydrophobicity and catalyst, we realized electricity generation for a long duration, which could last for 26 000 s after adding H2O2 only once. We believe this work provides a simple process for the development of horizontal motion and provides a new path for energy reutilization. PMID:27093949

  17. Effect of nickel loading on hydrogen production and chemical oxygen demand (COD) destruction from glucose oxidation and gasification in supercritical water

    International Nuclear Information System (INIS)

    minutes of reaction time increased the hydrogen yield from 0.618 mol/mol to 1.45 mol/mol. Chemical oxygen demand (COD) removal efficiency was 75 % in presence of both commercial and synthesized catalysts and 90 % without catalyst. This study showed that the same hydrogen yield can be obtained from the synthesized low nickel alumina loading (18 wt %) catalyst with (65 wt %) nickel on silica-alumina loading commercial catalyst. (author)

  18. The reactivity of [PhP(Se)(mu-Se)]2 and (PhP)3Se2 towards acetylenes and cyanamides: X-ray crystal structures of some P-Se-C and P-Se-C-N heterocycles.

    Science.gov (United States)

    Bhattacharyya, Pravat; Slawin, Alexandra M Z; Woollins, J Derek

    2002-06-17

    Several unusual P-Se-C and P-Se-C-N heterocycles are formed by the reaction of [PhP(Se)(mu-Se)]2 or (PhP)3Se2 with alkynes or cyanamides, generated by the fragmentation of the organophosphorus-selenium compound and addition across the C identical to C or C identical to N triple bond of the organic substrate. X-ray crystallographic analysis reveals an unexpected diversity of structural motifs within these heterocyclic systems, including P2SeCN, P2C2Se and PC2Se2 rings.

  19. Pretreatment of bottom sludge of crude oil storage tanks using chemical oxidation process with hydrogen peroxide and Fenton

    Directory of Open Access Journals (Sweden)

    Ramin Nabizadeh

    2014-05-01

    Conclusions: Mere application of chemical oxidation is not capable of complete treatment of the sludge but it is an effective process as a pre-treatment step for decreasing toxicity and increasing its biodegradability.

  20. The protein amide {sup 1}H{sup N} chemical shift temperature coefficient reflects thermal expansion of the N-H{center_dot}{center_dot}{center_dot}O=C hydrogen bond

    Energy Technology Data Exchange (ETDEWEB)

    Hong Jingbo; Jing Qingqing; Yao Lishan, E-mail: yaols@qibebt.ac.cn [Chinese Academy of Sciences, Laboratory of Biofuels, Qingdao Institute of Bioenergy and Bioprocess Technology (China)

    2013-01-15

    The protein amide {sup 1}H{sup N} chemical shift temperature coefficient can be determined with high accuracy by recording spectra at different temperatures, but the physical mechanism responsible for this temperature dependence is not well understood. In this work, we find that this coefficient strongly correlates with the temperature coefficient of the through-hydrogen-bond coupling, {sup 3h}J{sub NC Prime }, based on NMR measurements of protein GB3. Parallel tempering molecular dynamics simulation suggests that the hydrogen bond distance variation at different temperatures/replicas is largely responsible for the {sup 1}H{sup N} chemical shift temperature dependence, from which an empirical equation is proposed to predict the hydrogen bond thermal expansion coefficient, revealing responses of individual hydrogen bonds to temperature changes. Different expansion patterns have been observed for various networks formed by {beta} strands.

  1. X-231B technology demonstration for in situ treatment of contaminated soil: Laboratory evaluation of chemical oxidation using hydrogen peroxide

    International Nuclear Information System (INIS)

    Treatability studies were conducted as part of a comprehensive research project initiated to demonstrate as well as evaluate in situ treatment technologies for volatile organic compounds (VOCs) and radioactive substances in wet, slowly permeable soils. The site of interest for this project was the X-231B Oil Biodegradation unit at the Portsmouth Gaseous Diffusion Plant, a US Department of Energy (DOE) facility in southern Ohio. This report describes the treatability studies that investigated the feasibility of the application of low-strength hydrogen peroxide (H2O2) solutions to treat trichloroethylene (TCE)-contaminated soil

  2. Treatment of odorous sulphur compounds by chemical scrubbing with hydrogen peroxide--stabilisation of the scrubbing solution.

    Science.gov (United States)

    Charron, Isabelle; Couvert, Annabelle; Laplanche, Alain; Renner, Christophe; Patria, Lucie; Requieme, Benoît

    2006-12-15

    To slow down the hydrogen peroxide decomposition in basic aqueous conditions, the addition of stabilizers and co-stabilizers in the scrubbing solution was investigated. Results found with sodium silicate (Na2SiO3) were quite promising but several problems still remained. Based on these observations, this study focused on the research of a better stabilizer. Several ways were investigated: the use of silicate solutions employed in pulp industries, the addition of co-stabilizers to sodium silicate, or the use of an another stabilizer (the poly-alpha-hydroxyacrylic acid). Experiments revealed that the poly-alpha-hydroxyacrylic acid is the best stabilizing compound.

  3. AB INITIO STUDY OF CHEMICAL ACTIVATION AND HYDROGENATION OF WHITE PHOSPHORUS IN REACTION WITH RHODIUM TRIHYDRIDE COMPLEX

    OpenAIRE

    Iolanta I. Balan; Natalia N. Gorinchoy

    2011-01-01

    The four-stage mechanism of reaction of the rhodium trihydride complex [(triphos)RhH3] (triphos=1,1,1-tris(diphenylphosphanylmethyl)ethane) with the white phosphorus molecule resulting in the phosphane and the cyclo-P3 complex [(triphos)M(η3-P3] is analyzed on the basis of ab initio calculations of reactants, products, and intermediate complexes of reaction. It is shown that generation of the transient complex [(triphos)RhH(η1:η1-P4)] followed by intramolecular hydrogen atom migration from t...

  4. A Microscale Approach to Chemical Kinetics in the General Chemistry Laboratory: The Potassium Iodide Hydrogen Peroxide Iodine-Clock Reaction

    Science.gov (United States)

    Sattsangi, Prem D.

    2011-01-01

    A microscale laboratory for teaching chemical kinetics utilizing the iodine clock reaction is described. Plastic pipets, 3 mL volume, are used to store and deliver precise drops of reagents and the reaction is run in a 24 well plastic tray using a total 60 drops of reagents. With this procedure, students determine the rate of reaction and the…

  5. Influence of Fe-doped on structural, electronic structural and optical properties of hydrogenated amorphous carbon films prepared by plasma enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    Fe-doped hydrogenated amorphous carbon (a-C:H:Fe) films were deposited from an isobutene/ferrocene/H2 gas mixture by plasma enhanced chemical metal organic vapor deposition. Raman spectra were used to characterize the bonding structure of the a-C:H:Fe films and hydrogenated amorphous carbon (a-C:H) films. Optical properties were investigated by the UV-vis spectroscopy and the photoluminescence spectra. The number of six-numbered rings of the a-C:H films increases and sp2 clustering of the films decreases after Fe-doping. The Tauc optical gap of the a-C:H:Fe films becomes narrower by 0.15-0.23 eV relative to the value of the a-C:H films. The narrowing of the optical gap after doping is attributed primarily to the extended state around the Fe deep level in the band gap and the narrowing of the π and π* band edge states because of the increase of the number of six-numbered rings in the a-C:H films. Fe deep level defects of the a-C:H:Fe films contribute chiefly to non-radiative recombination.

  6. Preparation of high-quality hydrogenated amorphous silicon film with a new microwave electron cyclotron resonance chemical vapour deposition system assisted with hot wire

    Institute of Scientific and Technical Information of China (English)

    Zhu Xiu-Hong; Chen Guang-Hua; Yin Sheng-Yi; Rong Yan-Dong; Zhang Wen-Li; Hu Yue-Hui

    2005-01-01

    The preparation of high-quality hydrogenated amorphous silicon (a-Si:H) film with a new microwave electron cyclotron resonance-chemical vapour deposition (MWECR-CVD) system assisted with hot wire is presented. In this system the hot wire plays an important role in perfecting the microstructure as well as improving the stability and the optoelectronic properties of the a-Si:H film. The experimental results indicate that in the microstructure of the a-Si:H film, the concentration of dihydride is decreased and a trace of microcrystalline occurs, which is useful to improve its stability, and that in the optoelectronic properties of the a-Si:H film, the deposition rate reaches above 2.0nm/s and the photosensitivity increases up to 4.71× 105.

  7. Gas barrier properties of hydrogenated amorphous carbon films coated on polymers by surface-wave plasma chemical vapor deposition

    International Nuclear Information System (INIS)

    Gas barrier characteristics of hydrogenated amorphous carbon (a-C:H) thin films coated on polymer sheets using the large-area surface-wave plasma (SWP) were studied. With SWP in He and CH4 gas mixture, a-C:H films were deposited over about 100 mm in diameter on high density polyethylene or polyethylene terephthalate (PET) sheets at temperature less than 70 deg. C. Experimental results show that gas permeation in the case of a-C:H film coating on PET sheet was reduced by a factor of more than 150 (0.27 cm3/m2 day atm), compared with that before coating. Plasma characteristics of SWP, such as electron density and electron energy distribution functions, and other film characteristics measured with Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy and atomic force microscope are presented and discussed

  8. Hydrogen bond driven chemical reactions: Beckmann rearrangement of cyclohexanone oxime into epsilon-caprolactam in supercritical water.

    Science.gov (United States)

    Boero, Mauro; Ikeshoji, Tamio; Liew, Chee Chin; Terakura, Kiyoyuki; Parrinello, Michele

    2004-05-26

    Recent experiments have shown that supercritical water (SCW) has the ability to accelerate and make selective synthetic organic reactions, thus replacing the common but environmentally harmful acid and basic catalysts. In an attempt to understand the intimate mechanism behind this observation, we analyze, via first-principles molecular dynamics, the Beckmann rearrangement of cyclohexanone oxime into epsilon-caprolactam in supercritical water, for which accurate experimental evidence has been reported. Differences in the wetting of the hydrophilic parts of the solute, enhanced by SCW, and the disrupted hydrogen bond network are shown to be crucial in triggering the reaction and in making it selective. Furthermore, the enhanced concentrations of H(+) in SCW play an important role in starting the reaction.

  9. Hydrogen production by Cyanobacteria

    Directory of Open Access Journals (Sweden)

    Chaudhuri Surabhi

    2005-12-01

    Full Text Available Abstract The limited fossil fuel prompts the prospecting of various unconventional energy sources to take over the traditional fossil fuel energy source. In this respect the use of hydrogen gas is an attractive alternate source. Attributed by its numerous advantages including those of environmentally clean, efficiency and renew ability, hydrogen gas is considered to be one of the most desired alternate. Cyanobacteria are highly promising microorganism for hydrogen production. In comparison to the traditional ways of hydrogen production (chemical, photoelectrical, Cyanobacterial hydrogen production is commercially viable. This review highlights the basic biology of cynobacterial hydrogen production, strains involved, large-scale hydrogen production and its future prospects. While integrating the existing knowledge and technology, much future improvement and progress is to be done before hydrogen is accepted as a commercial primary energy source.

  10. Determination of the effective mechanism of chemically stimulated diffusion in semiconductors at their interaction with an atomic hydrogen

    International Nuclear Information System (INIS)

    Paper is devoted to calculate coefficients of chemically stimulated diffusion (CSD) of some impurities in near-the-surface layers of germanium and gallium arsenide following well-known mechanisms to determine governing mechanism of CSD depending on type of diffusing impurity and conditions to carry out experiment. Calculation results of CSD coefficients following the mentioned mechanisms for copper in germanium showed that their efficiency was rather unimpressive in contrast to CSD mechanisms associated with energy transfer to crystal atomic subsystem

  11. Hydrogen energy systems studies

    Energy Technology Data Exchange (ETDEWEB)

    Ogden, J.M.; Kreutz, T.G.; Steinbugler, M. [Princeton Univ., NJ (United States)] [and others

    1996-10-01

    In this report the authors describe results from technical and economic assessments carried out during the past year with support from the USDOE Hydrogen R&D Program. (1) Assessment of technologies for small scale production of hydrogen from natural gas. Because of the cost and logistics of transporting and storing hydrogen, it may be preferable to produce hydrogen at the point of use from more readily available energy carriers such as natural gas or electricity. In this task the authors assess near term technologies for producing hydrogen from natural gas at small scale including steam reforming, partial oxidation and autothermal reforming. (2) Case study of developing a hydrogen vehicle refueling infrastructure in Southern California. Many analysts suggest that the first widespread use of hydrogen energy is likely to be in zero emission vehicles in Southern California. Several hundred thousand zero emission automobiles are projected for the Los Angeles Basin alone by 2010, if mandated levels are implemented. Assuming that hydrogen vehicles capture a significant fraction of this market, a large demand for hydrogen fuel could evolve over the next few decades. Refueling a large number of hydrogen vehicles poses significant challenges. In this task the authors assess near term options for producing and delivering gaseous hydrogen transportation fuel to users in Southern California including: (1) hydrogen produced from natural gas in a large, centralized steam reforming plant, and delivered to refueling stations via liquid hydrogen truck or small scale hydrogen gas pipeline, (2) hydrogen produced at the refueling station via small scale steam reforming of natural gas, (3) hydrogen produced via small scale electrolysis at the refueling station, and (4) hydrogen from low cost chemical industry sources (e.g. excess capacity in refineries which have recently upgraded their hydrogen production capacity, etc.).

  12. Optical and passivating properties of hydrogenated amorphous silicon nitride deposited by plasma enhanced chemical vapour deposition for application on silicon solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Wight, Daniel Nilsen

    2008-07-01

    quality, etch rate. The response of these parameters to high temperature anneals were correlated with structural changes in the silicon nitride films as measured by using the hydrogen bond concentration. Plasma enhanced chemical vapour deposition allows continuous variation in nearly all deposition parameters. The parameters studied in this work are the gas flow ratios and excitation power. In both direct and remote deposition systems, the increase in deposition power density lead to higher activation of ammonia which in turn lead to augmented incorporation of nitrogen into the films and thus lower refractive index. For a direct system, the same parameter change lead to a drastic fall in passivation quality of Czochralski silicon attributed to an increase in ion bombardment as well as the general observation that as deposited passivation tends to increase with refractive index. Silicon nitride films with variations in refractive index were also made by varying the silane-to-ammonia gas flow ratio. This simple parameter adjustment makes plasma enhanced chemical vapour deposited silicon nitride applicable to double layer anti-reflective coatings simulated in this work. The films were found to have an etch rate in 5% hydrofluoric acid that decreased with increasing refractive index. This behaviour is attributed to the decreasing concentration of nitrogen-to-hydrogen bonds in the films. Such bonds at the surface of silicon nitride have been suggested to be involved in the main reaction mechanism when etching silicon nitride in hydrofluoric acid. Annealing the films lead to a drastic fall in etch rates and was linked to the release of hydrogen from the nitrogen-hydrogen bonds. (author). 115 refs., 35 figs., 6 tabs

  13. Method and system for hydrogen evolution and storage

    Science.gov (United States)

    Thorn, David L.; Tumas, William; Hay, P. Jeffrey; Schwarz, Daniel E.; Cameron, Thomas M.

    2012-12-11

    A method and system for storing and evolving hydrogen (H.sub.2) employ chemical compounds that can be hydrogenated to store hydrogen and dehydrogenated to evolve hydrogen. A catalyst lowers the energy required for storing and evolving hydrogen. The method and system can provide hydrogen for devices that consume hydrogen as fuel.

  14. AB INITIO STUDY OF CHEMICAL ACTIVATION AND HYDROGENATION OF WHITE PHOSPHORUS IN REACTION WITH RHODIUM TRIHYDRIDE COMPLEX

    Directory of Open Access Journals (Sweden)

    Iolanta I. Balan

    2011-12-01

    Full Text Available The four-stage mechanism of reaction of the rhodium trihydride complex [(triphosRhH3] (triphos=1,1,1-tris(diphenylphosphanylmethylethane with the white phosphorus molecule resulting in the phosphane and the cyclo-P3 complex [(triphosM(η3-P3] is analyzed on the basis of ab initio calculations of reactants, products, and intermediate complexes of reaction. It is shown that generation of the transient complex [(triphosRhH(η1:η1-P4] followed by intramolecular hydrogen atom migration from the metal to one of the phosphorus atoms is the energetically favourable process. Calculations also show that P4 molecule is activated by coordination to the above complex: the metal-bonded P-P edge is broken, and the tetrahedron P4 is opened to form the butterfly geometry. This activation is realized mainly due to the one-orbital back donation of 4d-electron density from the atom of Rh to the unoccupied antibonding triple degenerate t1*-MO of P4.

  15. Optimization and application of atmospheric pressure chemical and photoionization hydrogen-deuterium exchange mass spectrometry for speciation of oxygen-containing compounds.

    Science.gov (United States)

    Acter, Thamina; Kim, Donghwi; Ahmed, Arif; Jin, Jang Mi; Yim, Un Hyuk; Shim, Won Joon; Kim, Young Hwan; Kim, Sunghwan

    2016-05-01

    This paper presents a detailed investigation of the feasibility of optimized positive and negative atmospheric pressure chemical ionization (APCI) mass spectrometry (MS) and atmospheric pressure photoionization (APPI) MS coupled to hydrogen-deuterium exchange (HDX) for structural assignment of diverse oxygen-containing compounds. The important parameters for optimization of HDX MS were characterized. The optimized techniques employed in the positive and negative modes showed satisfactory HDX product ions for the model compounds when dichloromethane and toluene were employed as a co-solvent in APCI- and APPI-HDX, respectively. The evaluation of the mass spectra obtained from 38 oxygen-containing compounds demonstrated that the extent of the HDX of the ions was structure-dependent. The combination of information provided by different ionization techniques could be used for better speciation of oxygen-containing compounds. For example, (+) APPI-HDX is sensitive to compounds with alcohol, ketone, or aldehyde substituents, while (-) APPI-HDX is sensitive to compounds with carboxylic functional groups. In addition, the compounds with alcohol can be distinguished from other compounds by the presence of exchanged peaks. The combined information was applied to study chemical compositions of degraded oils. The HDX pattern, double bond equivalent (DBE) distribution, and previously reported oxidation products were combined to predict structures of the compounds produced from oxidation of oil. Overall, this study shows that APCI- and APPI-HDX MS are useful experimental techniques that can be applied for the structural analysis of oxygen-containing compounds.

  16. Hydrogen technologies

    International Nuclear Information System (INIS)

    To the non-nonsense engineer, any talk of a hydrogen economy may seem like so much hot air. This paper reports that as legislative, safety and environmental issues continue to tighten, they're promoting hydrogen's chances as an energy source and, more immediately, its prospects as a chemical feedstock. Paradoxically, the environmental demands that are stimulating hydrogen demand are also inhibiting the gas's production. Previously, gasoline was made with benzene, which means that H2 was rejected. But now that the laws mandate lower aromatic and higher oxygenate levels in gasolines, there's less H2 available as byproduct. At the same time, H2 demand is rising in hydrodesulfurization units, since the same laws require refiners to cut sulfur levels in fuels. Supplementary sources for the gas are also shrinking. In the chlor-alkali industry, H2 output is dropping, as demand for its coproduct chlorine weakens. At the same time, H2 demand for the making of hydrogen peroxide is growing, as that environmentally safer bleach gains chlorine's market share

  17. Analysis of nonequilibrium chemical processes in the plume of subsonic and supersonic aircraft with hydrogen and hydrocarbon combustion engine

    Energy Technology Data Exchange (ETDEWEB)

    Starik, A.M.; Lebedev, A.B.; Titova, N.S. [Central Inst. of Aviation Motors, Moscow (Russian Federation)

    1997-12-31

    On the basic of quasi one dimensional mixing model the numerical analysis of nonequilibrium chemical processes in the plume of subsonic and hypersonic aircraft is presented. It was found that species HNO, HNO{sub 3}, HNO{sub 4}, N{sub 2}O{sub 5}, ClO{sub 2}, CH{sub 3}NO{sub 2} could be formed as a result of nonequilibrium processes in the plume and their concentrations can essentially exceed both background values in free stream of atmosphere and their values at the nozzle exit plane. (author) 10 refs.

  18. Chemical and enzymatic approaches for 11C-labelled octopamine synthesis using hydrogen [11C]cyanide

    International Nuclear Information System (INIS)

    Octopamine, the β-hydroxy derivative of tyramine, has been the objects of growing interest as biogenic trace amine. Studies using [3H]-labelled p- and m-octopamine have shown that they are both taken up in noradrenergic nerve terminals, accumulated in storage vesicles, and released together with noradrenaline on stimulation. p- and m-[11C]Octopamine have been synthesized from H[11C]CN in two-step sequence. Both chemical and enzymatic procedures have been used for the production of [11C]cyanohydrin intermediates as the key step. The enantiomeric composition of the labelled products obtained through the enzymatic process was assayed by analytical HPLC

  19. Experiments on interactions between zirconium-containing melt and water (ZREX): Hydrogen generation and chemical augmentation of energetics

    Energy Technology Data Exchange (ETDEWEB)

    Cho, D.H.; Armstrong, D.R.; Gunther, W.H. [Argonne National Lab., IL (United States); Basu, S. [Nuclear Regulatory Commission, Washington, DC (United States)

    1997-08-01

    The results of the first data series of experiments on interactions between zirconium-containing melt and water are described. These experiments involved dropping 1-kg batches of pure zirconium or zirconium-zirconium dioxide mixture melt into a column of water. A total of nine tests were conducted, including four with pure zirconium melt and five with Zr-ZrO{sub 2} mixture melt. Explosions took place only in those tests which were externally triggered. While the extent of zirconium oxidation in the triggered experiments was quite extensive, the estimated explosion energetics were found to be very small compared to the combined thermal and chemical energy available.

  20. Experiments on interactions between zirconium-containing melt and water (ZREX). Hydrogen generation and chemical augmentation of energetics

    Energy Technology Data Exchange (ETDEWEB)

    Cho, D.H.; Armstrong, D.R.; Gunther, W.H. [Argonne National Lab., IL (United States); Basu, S.

    1998-01-01

    The results of the first data series of experiments on interactions between zirconium-containing melt and water are described. These experiments involved dropping 1-kg batches of pure zirconium or zirconium-zirconium dioxide mixture melt into a column of water. A total of nine tests were conducted, including four with pure zirconium melt and five with Zr-ZrO{sub 2} mixture melt. Explosions took place only in those tests which were externally triggered. While the extent of zirconium oxidation in the triggered experiments was quite extensive, the estimated explosion energetics were found to be very small compared to the combined thermal and chemical energy available. (author)

  1. Chemical and structural analysis of solvothermal synthesized tungsten oxide nanotube without template and its hydrogen sensitive property

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Taisheng; Zhang, Yue, E-mail: zhangy@buaa.edu.cn; Li, Chen

    2014-01-25

    Graphical abstract: Imaged models of formation of nanotube during crystal growth: (a) precursor react with each other; (b) the crystal plane bended as crystallization; (c) the nanotube formed finally. Highlights: • The WO{sub 3} naonotube was prepared by solvothermal method without any addition. • The steric effect and the nucleation and growth mechanism resulted in the nanotube. • The nanotube film surface showed high oxygen vacancies. • The nanotube film showed diffusion dominated sensitivity. -- Abstract: Tungsten oxide nanotubes were synthesized by solvothermal process without template. The steric effect and the concentration of WCl{sub 6} are the dominant factors for the formation mechanism of the nanotube. The steric effect was experimentally and systematically studied with solvents including ethanol, isopropanol, n-propanol and butylalcohol, which have different molecular configuration and length, while the effect of concentration was investigated by characterizing the nanostructured productions. The samples have been investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). The surface chemistry of the nanotube is characterized by X-ray photoelectron spectroscopy (XPS). The results indicated that the solvents species and WCl{sub 6} concentration obviously diversified the morphologies of the products; the nanotubes synthesized with isopropanol composed of W{sub 18}O{sub 49} phase; the crystal defects (O atom vacancy) formed during rapid crystallization could be modified by heat treatment. The DC electrical response of the nanotube thin film to hydrogen was measured the temperature range from 200 °C to 300 °C, which indicated a decline in electrical resistance with good sensitivity, and showed the mechanism that the reaction limited process works at low temperature, whereas the diffusion limited process works at higher temperature.

  2. Effects of various chemical compounds on spontaneous and hydrogen peroxide-induced reversion in strain TA104 of Salmonella typhimurium.

    Science.gov (United States)

    Han, J S

    1992-04-01

    In experiments designed to determine which active oxygen species contribute to hydrogen peroxide (HP)-induced reversion in strain TA104 of Salmonella typhimurium, 1,10-phenanthroline (an iron chelator, which prevents the formation of hydroxyl radicals from HP and DNA-bound iron by the Fenton reaction), sodium azide (a singlet oxygen scavenger), and potassium iodide (an hydroxyl radical scavenger) inhibited HP-induced reversion. These results indicate that hydroxyl radicals generated from HP by the Fenton reaction, and perhaps singlet oxygen, contribute to HP-induced reversion in TA104. However, reduced glutathione (reduces Fe3+ to Fe2+ and/or HP to water), diethyldithiocarbamic acid (an inhibitor of superoxide dismutase), diethyl maleate (a glutathione scavenger), and 3-amino-1,2,4-triazole (an inhibitor of catalase) did not inhibit HP-induced reversion in TA104. Thus, superoxide radical anions and HP itself do not appear to be the cause of HP-induced reversion in this strain. In experiments on the effect of 5 common dietary compounds (beta-carotene, retinoic acid, and vitamins A, C and E), chlorophyllin (CHL), and ergothioneine, the frequency of revertants in TA104 increased above the spontaneous frequency in the presence of beta-carotene or vitamin C (about 2-fold) or vitamin A (about 3-fold). The 5 dietary antimutagens and CHL did not inhibit HP-induced reversion in TA104. However, L-ergothioneine inhibited HP-induced reversion in this strain. Therefore, it is likely that L-ergothioneine is a scavenger of hydroxyl radicals or an inhibitor of their formation, and perhaps of singlet oxygen, at the concentrations tested in TA104.

  3. Short communication: Chemical composition, fatty acid composition, and sensory characteristics of Chanco cheese from dairy cows supplemented with soybean and hydrogenated vegetable oils.

    Science.gov (United States)

    Vargas-Bello-Pérez, E; Fehrmann-Cartes, K; Íñiguez-González, G; Toro-Mujica, P; Garnsworthy, P C

    2015-01-01

    Lipid supplements can be used to alter fatty acid (FA) profiles of dairy products. For Chanco cheese, however, little information is available concerning effects of lipid supplements on sensorial properties. The objective of this study was to examine effects of supplementation of dairy cow diets with soybean (SO) and hydrogenated vegetable (HVO) oils on chemical and FA composition of milk and cheese and sensory characteristics of cheese. Nine multiparous Holstein cows averaging 169±24d in milk at the beginning of the study were used in a replicated (n=3) 3×3 Latin square design that included 3 periods of 21d. All cows received a basal diet formulated with a 56:44 forage:concentrate ratio. Dietary treatments consisted of the basal diet (control; no fat supplement), and the basal diet supplemented with SO (unrefined oil; 500g/d per cow) and HVO (manufactured from palm oil; 500g/d per cow). Milk fat yield was lower with HVO compared with control and SO. Cheese chemical composition and sensory profile were not affected by dietary treatment. Vaccenic (C18:1 trans-11) and oleic (C18:1 cis-9) acids were higher for SO than for control and HVO. Compared with control and HVO, SO decreased saturated FA and increased monounsaturated FA. The thrombogenic index of milk and cheese produced when cows were fed SO was lower than when cows were fed on control and HVO. The outcome of this study showed that, compared with control and HVO, supplementing dairy cow diets with SO improves milk and cheese FA profile without detrimental effects on the chemical composition of milk and cheese and the sensory characteristics of cheese.

  4. Properties of Erbium Doped Hydrogenated Amorphous Carbon Layers Fabricated by Sputtering and Plasma Assisted Chemical Vapor Deposition

    Directory of Open Access Journals (Sweden)

    V. Prajzler

    2008-01-01

    Full Text Available We report about properties of carbon layers doped with Er3+ ions fabricated by Plasma Assisted Chemical Vapor Deposition (PACVD and by sputtering on silicon or glass substrates. The structure of the samples was characterized by X-ray diffraction and their composition was determined by Rutherford Backscattering Spectroscopy and Elastic Recoil Detection Analysis. The Absorbance spectrum was taken in the spectral range from 400 nm to 600 nm. Photoluminescence spectra were obtained using two types of Ar laser (λex=514.5 nm, lex=488 nm and also using a semiconductor laser (λex=980 nm. Samples fabricated by magnetron sputtering exhibited typical emission at 1530 nm when pumped at 514.5 nm. 

  5. ERDA's Chemical Energy Storage Program

    Science.gov (United States)

    Swisher, J. H.; Kelley, J. H.

    1977-01-01

    The Chemical Energy Storage Program is described with emphasis on hydrogen storage. Storage techniques considered include pressurized hydrogen gas storage, cryogenic liquid hydrogen storage, storage in hydride compounds, and aromatic-alicyclic hydrogen storage. Some uses of energy storage are suggested. Information on hydrogen production and hydrogen use is also presented. Applications of hydrogen energy systems include storage of hydrogen for utilities load leveling, industrial marketing of hydrogen both as a chemical and as a fuel, natural gas supplementation, vehicular applications, and direct substitution for natural gas.

  6. Understanding the conformational impact of chemical modifications on monoclonal antibodies with diverse sequence variation using hydrogen/deuterium exchange mass spectrometry and structural modeling.

    Science.gov (United States)

    Zhang, Aming; Hu, Ping; MacGregor, Paul; Xue, Yu; Fan, Haihong; Suchecki, Peter; Olszewski, Leonard; Liu, Aston

    2014-04-01

    Chemical modifications can potentially induce conformational changes near the modification site and thereby impact the safety and efficacy of protein therapeutics. Hydrogen/deuterium exchange mass spectrometry (HDX-MS) has emerged as a powerful analytical technique with high spatial resolution and sensitivity in detecting such local conformational changes. In this study, we utilized HDX-MS combined with structural modeling to examine the conformational impact on monoclonal antibodies (mAbs) caused by common chemical modifications including methionine (Met) oxidation, aspartic acid (Asp) isomerization, and asparagine (Asn) deamidation. Four mAbs with diverse sequences and glycosylation states were selected. The data suggested that the impact of Met oxidation was highly dependent on its location and glycosylation state. For mAbs with normal glycosylation in the Fc region, oxidation of the two conserved Met252 and Met428 (Kabat numbering) disrupted the interface interactions between the CH2 and CH3 domains, thus leading to a significant decrease in CH2 domain thermal stability as well as a slight increase in aggregation propensity. In contrast, Met oxidation in the variable region and CH3 domain had no detectable impact on mAb conformation. For aglycosylated mAb, Met oxidation could cause a more global conformational change to the whole CH2 domain, coincident with the larger decrease in thermal stability and significant increase in aggregation rate. Unlike Met oxidation, Asn deamidation and Asp isomerization mostly had very limited effects on mAb conformation, with the exception of succiminide intermediate formation which induced a measurable local conformational change to be more solvent protected. Structural modeling suggested that the succinimide intermediate was stabilized by adjacent aromatic amino acids through ring-ring stacking interactions. PMID:24597564

  7. Chemical activation in Rhinella arenarum oocytes: effect of dehydroleucodine (DhL) and its hydrogenated derivative (2H-DhL).

    Science.gov (United States)

    Medina, M F; Bühler, M I; Sánchez-Toranzo, G

    2015-12-01

    Mature oocytes are arrested in metaphase II due to the presence of high levels of active maturation promoting factor (MPF). After fertilization, active MPF levels decline abruptly, enabling oocytes to complete meiosis II. One of the first and universal events of oocyte activation is an increase in cytosolic Ca2+ that would be responsible for MPF inactivation. Mature oocytes can also be activated by parthenogenetic activation. The aims of this work are to test the ability of dehydroleucodine (DhL) and its hydrogenated derivative 11,13-dihydro-dehydroleucodine (2H-DhL) to induce chemical activation in amphibian oocytes and to study the participation of calcium in the process. Results indicated that DhL and 2H-DhL induced oocyte activation in a dose-dependent manner. After 90 min of treatment, DhL 36 μM was able to induce 95% activation, while 2H-DhL 36 μM was less active, with only 40% activation. Our results suggest that DhL induced the inhibition of MPF activity, probably by an increase in intracellular Ca2+ concentration. Extracellular Ca2+ would not be significant, although Ca2+ release from intracellular stores is critical. In this sense, IP3Rs and RyRs were involved in the Ca2+ transient induced by lactones. In this species, RyRs appears to be the largest contributor to Ca2+ release in DhL-induced activation. Although more studies are needed on the mechanism of action through which these lactones induce oocyte activation in Rhinella arenarum, the results of this research provide interesting perspectives for the use of these lactones as chemical activators in in vitro fertilization and cloning.

  8. Hydrogenated amorphous carbon-nitride films deposited on Si(100) by direct-current saddle-field plasma-enhanced chemical-vapor deposition

    CERN Document Server

    Jang, H K; Lee, Y S; Whangbo, S W; Whang, C N; Yoo, Y Z; Kim, H G

    1999-01-01

    Hydrogenated amorphous carbon nitride [a-C:H(N)] films were deposited using dc saddle-field plasma-enhanced chemical-vapor deposition. The structural and the compositional changes induced in the films by the different flow-rate ratios of N sub 2 to CH sub 4 (n sub N sub 2 /n sub C sub H sub sub 4) were investigated using Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The deposition rate of the films abruptly decreased upon increasing the n sub N sub 2 /n sub C sub H sub sub 4 ratio. However, for n sub N sub 2 /n sub C sub H sub sub 4 >0.5, the deposition rate slightly decreased with increasing n sub N sub 2 /n sub C sub H sub sub 4. The ratio of N to C (N/C) of the films saturated to 0.25 with increasing n sub N sub 2 /n sub C sub H sub sub 4. The numbers of N-H and C ident to N bonds in the films increased with increasing n sub N sub 2 /n sub C sub H sub sub 4 , but the number of C-H bonds decreased. The optical band-gap energy of the films decreased from 2.53 eV to 2.3 eV as t...

  9. Hydrogen-oxygen flame acceleration and transition to detonation in channels with no-slip walls for a detailed chemical reaction model.

    Science.gov (United States)

    Ivanov, M F; Kiverin, A D; Liberman, M A

    2011-05-01

    The features of flame acceleration in channels with wall friction and the deflagration to detonation transition (DDT) are investigated theoretically and using high resolution numerical simulations of two-dimensional reactive Navier-Stokes equations, including the effects of viscosity, thermal conduction, molecular diffusion, and a detailed chemical reaction mechanism for hydrogen-oxygen gaseous mixture. It is shown that in a wide channel, from the beginning, the flame velocity increases exponentially for a short time and then flame acceleration decreases, ending up with the abrupt increase of the combustion wave velocity and the actual transition to detonation. In a thin channel with a width smaller than the critical value, the exponential increase of the flame velocity is not bounded and ends up with the transition to detonation. The transition to detonation occurs due to the pressure pulse, which is formed at the tip of the accelerating flame. The amplitude of the pressure pulse grows exponentially due to a positive feedback coupling between the pressure pulse and the heat released in the reaction. Finally, large amplitude pressure pulse steepens into a strong shock coupled with the reaction zone forming the overdriven detonation. The evolution from a temperature gradient to a detonation via the Zeldovich gradient mechanism and its applicability to the deflagration-to-detonation transition is investigated for combustible materials whose chemistry is governed by chain-branching kinetics. The results of the high resolution simulations are fully consistent with experimental observations of the flame acceleration and DDT.

  10. Structure, mechanical, and frictional properties of hydrogenated fullerene-like amorphous carbon film prepared by direct current plasma enhanced chemical vapor deposition

    Science.gov (United States)

    Wang, Yongfu; Gao, Kaixiong; Zhang, Junyan

    2016-07-01

    In this study, fullerene like carbon (FL-C) is introduced in hydrogenated amorphous carbon (a-C:H) film by employing a direct current plasma enhanced chemical vapor deposition. The film has a low friction and wear, such as 0.011 and 2.3 × 10-9mm3/N m in the N2, and 0.014 and 8.4 × 10-8mm3/N m in the humid air, and high hardness and elasticity (25.8 GPa and 83.1%), to make further engineering applications in practice. It has several nanometers ordered domains consisting of less frequently cross-linked graphitic sheet stacks. We provide new evidences for understanding the reported Raman fit model involving four vibrational frequencies from five, six, and seven C-atom rings of FL-C structures, and discuss the structure evolution before or after friction according to the change in the 1200 cm-1 Raman band intensity caused by five- and seven-carbon rings. Friction inevitably facilitates the transformation of carbon into FL-C nanostructures, namely, the ultra low friction comes from both such structures within the carbon film and the sliding induced at friction interface.

  11. The influence of charge effect on the growth of hydrogenated amorphous silicon by the hot-wire chemical vapor deposition technique

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Q.; Nelson, B.P.; Iwaniczko, E.; Mahan, A.H.; Crandall, R.S.; Benner, J. [National Renewable Energy Lab., Golden, CO (United States)

    1998-09-01

    The authors observe at lower substrate temperatures that the scatter in the dark conductivity on hydrogenated amorphous silicon (a-Si:H) films grown on insulating substrates (e.g., Corning 7059 glass) by the hot-wire chemical vapor deposition technique (HWCVD) can be five orders of magnitude or more. This is especially true at deposition temperatures below 350 C. However, when the authors grow the same materials on substrates with a conductive grid, virtually all of their films have acceptable dark conductivity (< 5 {times} 10{sup {minus}10} S/cm) at all deposition temperatures below 425 C. This is in contrast to only about 20% of the materials grown in this same temperature range on insulating substrates having an acceptable dark conductivity. The authors estimated an average energy of 5 eV electrons reaching the growing surface in vacuum, and did additional experiments to see the influence of both the electron flux and the energy of the electrons on the film growth. Although these effects do not seem to be important for growing a-Si:H by HWCVD on conductive substrates, they help better understand the important parameters for a-Si:H growth, and thus, to optimize these parameters in other applications of HWCVD technology.

  12. Proposed replacement and operation of the anhydrous hydrogen fluoride supply and fluidized-bed chemical processing systems at Building 9212, Y-12 Plant, Oak Ridge, Tennessee

    International Nuclear Information System (INIS)

    The US Department of Energy (DOE) proposes to replace the existing anhydrous hydrogen fluoride (AHF) supply and fluidized-bed reactor systems for the Weapons Grade Highly Enriched Uranium Chemical Recovery and Recycle Facility, Building 9212, which is located within the Y-12 Plant on DOE's Oak Ridge Reservation in Oak Ridge, Tennessee. The proposed replacement system would be based upon modern design criteria and safety analyses. The replacement AHF supply and distribution system equipment would be located on the existing Dock 8/8A at Building 9212. Utilities would be extended to the dock to service the process equipment. The following process equipment modules would be prefabricated for installation at the modified dock: an AHF cylinder enclosure, an AHF supply manifold and vaporizer module, an AHF sump tank and transfer skid, and an AHF supply off-gas scrubber assembly module. The fluidized-bed reactor system would be constructed in an area adjacent to the existing system in Building 9212. The replacement equipment would consist of a new reduction fluidized-bed reactor, a hydrofluorination fluidized-bed reactor, and associated air emission control equipment. The no-action alternative, which is the continued operation of the existing AHF supply and fluidized-bed reactor systems, was also evaluated

  13. Characterization of amorphous hydrogenated carbon formed by low-pressure inductively coupled plasma enhanced chemical vapor deposition using multiple low-inductance antenna units.

    Science.gov (United States)

    Tsuda, Osamu; Ishihara, Masatou; Koga, Yoshinori; Fujiwara, Shuzo; Setsuhara, Yuichi; Sato, Naoyuki

    2005-03-24

    Three-dimensional plasma enhanced chemical vapor deposition (CVD) of hydrogenated amorphous carbon (a-C:H) has been demonstrated using a new type high-density volumetric plasma source with multiple low-inductance antenna system. The plasma density in the volume of phi 200 mm x 100 mm is 5.1 x 10(10) cm(-3) within +/-5% in the lateral directions and 5.2 x 10(10)cm(-3) within +/-10% in the axial direction for argon plasma under the pressure of 0.1 Pa and the total power as low as 400 W. The uniformity of the thickness and refractive index is within +/-3.5% and +/-1%, respectively, for the a-C:H films deposited on the substrates placed on the six side walls, the top of the phi 60 mm x 80 mm hexagonal substrate holder in the pure toluene plasma under the pressure is as low as 0.04 Pa, and the total power is as low as 300 W. It is also found that precisely controlled ion bombardment by pulse biasing led to the explicit observation in Raman and IR spectra of the transition from polymer-like structure to diamond-like structure accompanied by dehydrogenation due to ion bombardment. Moreover, it is also concluded that the pulse biasing technique is effective for stress reduction without a significant degradation of hardness. The stress of 0.6 GPa and the hardness of 15 GPa have been obtained for 2.0 microm thick films deposited with the optimized deposition conditions. The films are durable for the tribology test with a high load of 20 N up to more than 20,000 cycles, showing the specific wear rate and the friction coefficient were 1.2 x 10(-7) mm3/Nm and 0.04, respectively.

  14. Electrochemical hydrogen Storage Systems

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Digby Macdonald

    2010-08-09

    As the global need for energy increases, scientists and engineers have found a possible solution by using hydrogen to power our world. Although hydrogen can be combusted as a fuel, it is considered an energy carrier for use in fuel cells wherein it is consumed (oxidized) without the production of greenhouse gases and produces electrical energy with high efficiency. Chemical storage of hydrogen involves release of hydrogen in a controlled manner from materials in which the hydrogen is covalently bound. Sodium borohydride and aminoborane are two materials given consideration as chemical hydrogen storage materials by the US Department of Energy. A very significant barrier to adoption of these materials as hydrogen carriers is their regeneration from 'spent fuel,' i.e., the material remaining after discharge of hydrogen. The U.S. Department of Energy (DOE) formed a Center of Excellence for Chemical Hydrogen Storage, and this work stems from that project. The DOE has identified boron hydrides as being the main compounds of interest as hydrogen storage materials. The various boron hydrides are then oxidized to release their hydrogen, thereby forming a 'spent fuel' in the form of a lower boron hydride or even a boron oxide. The ultimate goal of this project is to take the oxidized boron hydrides as the spent fuel and hydrogenate them back to their original form so they can be used again as a fuel. Thus this research is essentially a boron hydride recycling project. In this report, research directed at regeneration of sodium borohydride and aminoborane is described. For sodium borohydride, electrochemical reduction of boric acid and sodium metaborate (representing spent fuel) in alkaline, aqueous solution has been investigated. Similarly to literature reports (primarily patents), a variety of cathode materials were tried in these experiments. Additionally, approaches directed at overcoming electrostatic repulsion of borate anion from the cathode, not

  15. Purdue Hydrogen Systems Laboratory

    International Nuclear Information System (INIS)

    The Hydrogen Systems Laboratory in a unique partnership between Purdue University's main campus in West Lafayette and the Calumet campus was established and its capabilities were enhanced towards technology demonstrators. The laboratory engaged in basic research in hydrogen production and storage and initiated engineering systems research with performance goals established as per the USDOE Hydrogen, Fuel Cells, and Infrastructure Technologies Program. In the chemical storage and recycling part of the project, we worked towards maximum recycling yield via novel chemical selection and novel recycling pathways. With the basic potential of a large hydrogen yield from AB, we used it as an example chemical but have also discovered its limitations. Further, we discovered alternate storage chemicals that appear to have advantages over AB. We improved the slurry hydrolysis approach by using advanced slurry/solution mixing techniques. We demonstrated vehicle scale aqueous and non-aqueous slurry reactors to address various engineering issues in on-board chemical hydrogen storage systems. We measured the thermal properties of raw and spent AB. Further, we conducted experiments to determine reaction mechanisms and kinetics of hydrothermolysis in hydride-rich solutions and slurries. We also developed a continuous flow reactor and a laboratory scale fuel cell power generation system. The biological hydrogen production work summarized as Task 4.0 below, included investigating optimal hydrogen production cultures for different substrates, reducing the water content in the substrate, and integrating results from vacuum tube solar collector based pre and post processing tests into an enhanced energy system model. An automated testing device was used to finalize optimal hydrogen production conditions using statistical procedures. A 3 L commercial fermentor (New Brunswick, BioFlo 115) was used to finalize testing of larger samples and to consider issues related to scale up. Efforts

  16. Purdue Hydrogen Systems Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Jay P Gore; Robert Kramer; Timothee L Pourpoint; P. V. Ramachandran; Arvind Varma; Yuan Zheng

    2011-12-28

    The Hydrogen Systems Laboratory in a unique partnership between Purdue University's main campus in West Lafayette and the Calumet campus was established and its capabilities were enhanced towards technology demonstrators. The laboratory engaged in basic research in hydrogen production and storage and initiated engineering systems research with performance goals established as per the USDOE Hydrogen, Fuel Cells, and Infrastructure Technologies Program. In the chemical storage and recycling part of the project, we worked towards maximum recycling yield via novel chemical selection and novel recycling pathways. With the basic potential of a large hydrogen yield from AB, we used it as an example chemical but have also discovered its limitations. Further, we discovered alternate storage chemicals that appear to have advantages over AB. We improved the slurry hydrolysis approach by using advanced slurry/solution mixing techniques. We demonstrated vehicle scale aqueous and non-aqueous slurry reactors to address various engineering issues in on-board chemical hydrogen storage systems. We measured the thermal properties of raw and spent AB. Further, we conducted experiments to determine reaction mechanisms and kinetics of hydrothermolysis in hydride-rich solutions and slurries. We also developed a continuous flow reactor and a laboratory scale fuel cell power generation system. The biological hydrogen production work summarized as Task 4.0 below, included investigating optimal hydrogen production cultures for different substrates, reducing the water content in the substrate, and integrating results from vacuum tube solar collector based pre and post processing tests into an enhanced energy system model. An automated testing device was used to finalize optimal hydrogen production conditions using statistical procedures. A 3 L commercial fermentor (New Brunswick, BioFlo 115) was used to finalize testing of larger samples and to consider issues related to scale up

  17. Hydrogen sulfide protects against chemical hypoxia-induced injury by inhibiting ROS-activated ERK1/2 and p38MAPK signaling pathways in PC12 cells.

    Directory of Open Access Journals (Sweden)

    Aiping Lan

    Full Text Available Hydrogen sulfide (H(2S has been proposed as a novel neuromodulator and neuroprotective agent. Cobalt chloride (CoCl(2 is a well-known hypoxia mimetic agent. We have demonstrated that H(2S protects against CoCl(2-induced injuries in PC12 cells. However, whether the members of mitogen-activated protein kinases (MAPK, in particular, extracellular signal-regulated kinase1/2(ERK1/2 and p38MAPK are involved in the neuroprotection of H(2S against chemical hypoxia-induced injuries of PC12 cells is not understood. We observed that CoCl(2 induced expression of transcriptional factor hypoxia-inducible factor-1 alpha (HIF-1α, decreased cystathionine-β synthase (CBS, a synthase of H(2S expression, and increased generation of reactive oxygen species (ROS, leading to injuries of the cells, evidenced by decrease in cell viability, dissipation of mitochondrial membrane potential (MMP , caspase-3 activation and apoptosis, which were attenuated by pretreatment with NaHS (a donor of H(2S or N-acetyl-L cystein (NAC, a ROS scavenger. CoCl(2 rapidly activated ERK1/2, p38MAPK and C-Jun N-terminal kinase (JNK. Inhibition of ERK1/2 or p38MAPK or JNK with kinase inhibitors (U0126 or SB203580 or SP600125, respectively or genetic silencing of ERK1/2 or p38MAPK by RNAi (Si-ERK1/2 or Si-p38MAPK significantly prevented CoCl(2-induced injuries. Pretreatment with NaHS or NAC inhibited not only CoCl(2-induced ROS production, but also phosphorylation of ERK1/2 and p38MAPK. Thus, we demonstrated that a concurrent activation of ERK1/2, p38MAPK and JNK participates in CoCl(2-induced injuries and that H(2S protects PC12 cells against chemical hypoxia-induced injuries by inhibition of ROS-activated ERK1/2 and p38MAPK pathways. Our results suggest that inhibitors of ERK1/2, p38MAPK and JNK or antioxidants may be useful for preventing and treating hypoxia-induced neuronal injury.

  18. Hydrogen in the Methanol Production Process

    Science.gov (United States)

    Kralj, Anita Kovac; Glavic, Peter

    2006-01-01

    Hydrogen is a very important industrial gas in chemical processes. It is very volatile; therefore, it can escape from the process units and its mass balance is not always correct. In many industrial processes where hydrogen is reacted, kinetics are often related to hydrogen pressure. The right thermodynamic properties of hydrogen can be found for…

  19. A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions.

    Science.gov (United States)

    Brack, Paul; Dann, Sandie; Wijayantha, K G Upul; Adcock, Paul; Foster, Simon

    2016-01-01

    There is a growing research interest in the development of portable systems which can deliver hydrogen on-demand to proton exchange membrane (PEM) hydrogen fuel cells. Researchers seeking to develop such systems require a method of measuring the generated hydrogen. Herein, we describe a simple, low-cost, and robust method to measure the hydrogen generated from the reaction of solids with aqueous solutions. The reactions are conducted in a conventional one-necked round-bottomed flask placed in a temperature controlled water bath. The hydrogen generated from the reaction in the flask is channeled through tubing into a water-filled inverted measuring cylinder. The water displaced from the measuring cylinder by the incoming gas is diverted into a beaker on a balance. The balance is connected to a computer, and the change in the mass reading of the balance over time is recorded using data collection and spreadsheet software programs. The data can then be approximately corrected for water vapor using the method described herein, and parameters such as the total hydrogen yield, the hydrogen generation rate, and the induction period can also be deduced. The size of the measuring cylinder and the resolution of the balance can be changed to adapt the setup to different hydrogen volumes and flow rates. PMID:27584581

  20. Hydrogen sensor

    Science.gov (United States)

    Duan, Yixiang; Jia, Quanxi; Cao, Wenqing

    2010-11-23

    A hydrogen sensor for detecting/quantitating hydrogen and hydrogen isotopes includes a sampling line and a microplasma generator that excites hydrogen from a gas sample and produces light emission from excited hydrogen. A power supply provides power to the microplasma generator, and a spectrometer generates an emission spectrum from the light emission. A programmable computer is adapted for determining whether or not the gas sample includes hydrogen, and for quantitating the amount of hydrogen and/or hydrogen isotopes are present in the gas sample.

  1. Tobacco and chemicals (image)

    Science.gov (United States)

    Some of the chemicals associated with tobacco smoke include ammonia, carbon dioxide, carbon monoxide, propane, methane, acetone, hydrogen cyanide and various carcinogens. Other chemicals that are associated with chewing ...

  2. Hydrogen as automotive fuel

    International Nuclear Information System (INIS)

    An assessment of the technical/economic feasibility of the use of hydrogen as an automotive fuel is made based on analyses of the following: the chemical- physical properties of hydrogen in relation to its use in internal combustion engines; the modifications necessary to adapt internal combustion engines to hydrogen use; hydrogen fuel injection systems - with water vapour injection, cryogenic injection, and the low or high pressure injection of hydrogen directly into the combustion chamber; the current commercialization status of hydrogen automotive fuels; energy efficiency ratings; environmental impacts; in-vehicle storage systems - involving the use of hydrides, high pressure systems and liquid hydrogen storage systems; performance in terms of pay-load ratio; autonomous operation; and operating costs. The paper concludes that, considering current costs for hydrogen fuel production, distribution and use, at present, the employment of hydrogen fuelled vehicles is feasible only in highly polluted urban environments where the innovative vehicle's air pollution abatement characteristics would justify its high operating costs as compared with those of conventional automotive alternatives

  3. New hydrogen technologies

    International Nuclear Information System (INIS)

    This report presents an overview of the overall hydrogen system. There are separate sections for production, distribution, transport, storage; and applications of hydrogen. The most important methods for hydrogen production are steam reformation of natural gas and electrolysis of water. Of the renewable energy options, production of hydrogen by electrolysis using electricity from wind turbines or by gasification of biomass were found to be the most economic for Finland. Direct use of this electricity or the production of liquid fuels from biomass will be competing alternatives. When hydrogen is produced in the solar belt or where there is cheap hydropower it must be transported over long distances. The overall energy consumed for the transport is from 25 to 40 % of the initial available energy. Hydrogen storage can be divided into stationary and mobile types. The most economic, stationary, large scale hydrogen storage for both long and short periods is underground storage. When suitable sites are not available, then pressure vessels are the best for short period and liquid H2 for long period. Vehicle storage of hydrogen is by either metal hydrides or liquid H2. Hydrogen is a very versatile energy carrier. It can be used to produce heat directly in catalytic burners without flame, to produce electricity in fuel cells with high efficiency for use in vehicles or for peak power shaving, as a fuel component with conventional fuels to reduce emissions, as a way to store energy and as a chemical reagent in reactions

  4. Photoelectrochemical hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Rocheleau, R.E.; Miller, E.; Misra, A. [Univ. of Hawaii, Honolulu, HI (United States)

    1996-10-01

    The large-scale production of hydrogen utilizing energy provided by a renewable source to split water is one of the most ambitious long-term goals of the U.S. Department of Energy`s Hydrogen Program. One promising option to meet this goal is direct photoelectrolysis in which light absorbed by semiconductor-based photoelectrodes produces electrical power internally to split water into hydrogen and oxygen. Under this program, direct solar-to-chemical conversion efficiencies as high as 7.8 % have been demonstrated using low-cost, amorphous-silicon-based photoelectrodes. Detailed loss analysis models indicate that solar-to-chemical conversion greater than 10% can be achieved with amorphous-silicon-based structures optimized for hydrogen production. In this report, the authors describe the continuing progress in the development of thin-film catalytic/protective coatings, results of outdoor testing, and efforts to develop high efficiency, stable prototype systems.

  5. Identification of N–H related acceptor defects in GaAsN grown by chemical beam epitaxy using hydrogen isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Elleuch, Omar, E-mail: mr.omar.elleuch@gmail.com; Wang, Li; Lee, Kan-Hua; Ikeda, Kazuma; Kojima, Nobuaki; Ohshita, Yoshio; Yamaguchi, Masafumi

    2015-11-15

    The N–H related acceptor defects in GaAsN grown by chemical beam epitaxy (CBE) are studied by hydrogen isotopes, H and D. When the films are grown by a conventional arsenic source, deep level transient spectroscopy (DLTS) reveals two energy levels at 0.11 and 0.19 eV above the valence band. These levels were considered to act as a double acceptor in the literature. When the films are grown by a deuterated arsenic source, new signals appear in DLTS spectra at 0.15 and 0.23 eV. This indicates that the new signals are originated from D-related defects. The energy differences between 0.15 and 0.11 eV, and that between 0.23 and 0.19 eV are same (0.04 eV). Although these energy levels become deeper with increasing the growth temperature, the energy differences are almost constant independent of the growth condition. In addition, the intensity ratios of the peaks at 0.15 (0.23) eV to that at 0.11 (0.19) eV have a good correlation with the isotopic concentration ratio of D to H in the grown films. Therefore, we conclude that the energy differences and intensity ratios of the DLTS peaks occur due to the structural change from N–H to N−D in the same type of defect, and that this acceptor is an N–H related defect. - Highlights: • The DLTS signals at 0.11 and 0.19 eV originate from a double acceptor. • Growth by D-TDMAAs: new defects that contain D are generated at 0.15 and 0.23 eV. • Energy differences between 0.15 (0.23) eV and 0.11 (0.19) eV: same, independent of T{sub G}. • Intensity ratios of peaks at 0.15 (0.23) eV to that at 0.11 (0.19) eV ≈ [D]/{[H]+[D]}. • Therefore, this acceptor is related to H.

  6. Geometrical criteria versus quantum chemical criteria for assessment of intramolecular hydrogen bond (IMHB) interaction: A computational comparison into the effect of chlorine substitution on IMHB of salicylic acid in its lowest energy ground state conformer

    Energy Technology Data Exchange (ETDEWEB)

    Paul, Bijan Kumar [Department of Chemistry, University of Calcutta, 92 A.P.C. Road, Calcutta 700009 (India); Guchhait, Nikhil, E-mail: nikhil.guchhait@rediffmail.com [Department of Chemistry, University of Calcutta, 92 A.P.C. Road, Calcutta 700009 (India)

    2013-02-01

    Highlights: ► Intramolecular hydrogen bonding (IMHB) in salicylic acid and its chloro derivatives. ► A complex effect of +R and −I effect of chlorine substituents on IMHB energy. ► Interplay between IMHB energy and aromaticity. ► Directional nature of IMHB from quantum chemical assessment. ► Quantum chemical treatment vs. geometrical criteria to assess weak interaction. - Abstract: Density functional theory based computational study has been performed to characterize intramolecular hydrogen bonding (IMHB) interaction in a series of salicylic acid derivatives varying in chlorine substitution on the benzene ring. The molecular systems studied are salicylic acid, 5-chlorosalicylic acid, 3,5-dichlorosalicylic acid and 3,5,6-tricholorosalicylic acid. Major emphasis is rendered on the analysis of IMHB interaction by calculation of electron density ρ(r) and Laplacian ∇{sup 2}ρ(r) at the bond critical point using atoms-in-molecule theory. Topological features, energy densities based on ρ(r) through perturbing the intramolecular H-bond distances suggest that at equilibrium geometry the IMHB interaction develops certain characteristics typical of covalent interaction. The interplay between aromaticity and resonance-assisted hydrogen bonding (RAHB) is discussed using both geometrical and magnetic criteria as the descriptors of aromaticity. The optimized geometry features, molecular electrostatic potential map analysis are also found to produce a consensus view in relation with the formation of RAHB in these systems.

  7. Chemical interesterification of soybean oil and fully hydrogenated soybean oil: Influence of the reaction time; Interesterificacao quimica de oleo de soja e oleo de soja totalmente hidrogenado: influencia do tempo de reacao

    Energy Technology Data Exchange (ETDEWEB)

    Ribeiro, Ana Paula Badan; Masuchi, Monise Helen; Grimaldi, Renato; Goncalves, Lireny Aparecida Guaraldo [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Fac. de Engenharia de Alimentos. Dept. de Tecnologia de Alimentos], e-mail: badanribeiro@yahoo.com.br

    2009-07-01

    Chemical interesterification is an important alternative to produce zero trans fats. In practice, however, excessive reaction times are used to ensure complete randomization. This work evaluated the influence of the reaction time on the interesterification of soybean oil/fully hydrogenated soybean oil blend, carried out in the following conditions: 100 deg C, 500 rpm stirring speed, 0.4% (w/w) sodium methoxide catalyst. The triacylglycerol composition, solid fat content and melting point analysis showed that the reaction was very fast, reaching the equilibrium within 5 min. This result suggests the interesterification can be performed in substantially lower times, with reduction in process costs. (author)

  8. Florida Hydrogen Initiative

    Energy Technology Data Exchange (ETDEWEB)

    Block, David L

    2013-06-30

    monitoring at any facility engaged in transport, handling and use of hydrogen. Development of High Efficiency Low Cost Electrocatalysts for Hydrogen Production and PEM Fuel Cell Applications ? M. Rodgers, Florida Solar Energy Center The objective of this project was to decrease platinum usage in fuel cells by conducting experiments to improve catalyst activity while lowering platinum loading through pulse electrodeposition. Optimum values of several variables during electrodeposition were selected to achieve the highest electrode performance, which was related to catalyst morphology. Understanding Mechanical and Chemical Durability of Fuel Cell Membrane Electrode Assemblies ? D. Slattery, Florida Solar Energy Center The objective of this project was to increase the knowledge base of the degradation mechanisms for membranes used in proton exchange membrane fuel cells. The results show the addition of ceria (cerium oxide) has given durability improvements by reducing fluoride emissions by an order of magnitude during an accelerated durability test. Production of Low-Cost Hydrogen from Biowaste (HyBrTec?) ? R. Parker, SRT Group, Inc., Miami, FL This project developed a hydrogen bromide (HyBrTec?) process which produces hydrogen bromide from wet-cellulosic waste and co-produces carbon dioxide. Eelectrolysis dissociates hydrogen bromide producing recyclable bromine and hydrogen. A demonstration reactor and electrolysis vessel was designed, built and operated. Development of a Low-Cost and High-Efficiency 500 W Portable PEMFC System ? J. Zheng, Florida State University, H. Chen, Bing Energy, Inc. The objectives of this project were to develop a new catalyst structures comprised of highly conductive buckypaper and Pt catalyst nanoparticles coated on its surface and to demonstrate fuel cell efficiency improvement and durability and cell cost reductions in the buckypaper based electrodes. Development of an Interdisciplinary Hydrogen and Fuel Cell Technology Academic Program ? J

  9. Large pressure range hydrogen sensor

    NARCIS (Netherlands)

    Boelsma, C.; Dam, B.

    2015-01-01

    The present invention relates to a thin-film sensor, to a method for producing a thin-film device, to an alloy for use in an optical sensing layer, to use of an alloy for sensing a chemical species such as hydrogen, to a sensor, to an apparatus for detecting hydrogen, to an electro-magnetic transfor

  10. Water's Hydrogen Bond Strength

    CERN Document Server

    Chaplin, Martin

    2007-01-01

    Water is necessary both for the evolution of life and its continuance. It possesses particular properties that cannot be found in other materials and that are required for life-giving processes. These properties are brought about by the hydrogen bonded environment particularly evident in liquid water. Each liquid water molecule is involved in about four hydrogen bonds with strengths considerably less than covalent bonds but considerably greater than the natural thermal energy. These hydrogen bonds are roughly tetrahedrally arranged such that when strongly formed the local clustering expands, decreasing the density. Such low density structuring naturally occurs at low and supercooled temperatures and gives rise to many physical and chemical properties that evidence the particular uniqueness of liquid water. If aqueous hydrogen bonds were actually somewhat stronger then water would behave similar to a glass, whereas if they were weaker then water would be a gas and only exist as a liquid at sub-zero temperature...

  11. Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    None

    2014-09-01

    This 2-page fact sheet provides a brief introduction to hydrogen production technologies. Intended for a non-technical audience, it explains how different resources and processes can be used to produce hydrogen. It includes an overview of research goals as well as “quick facts” about hydrogen energy resources and production technologies.

  12. Comparison of the regiospecific distribution from triacylglycerols after chemical and enzymatic interesterification of high oleic sunflower oil and fully hydrogenated high oleic sunflower oil blend by carbon-13 nuclear magnetic resonance.

    Science.gov (United States)

    Lopes, Thiago I B; Ribeiro, Marilene D M M; Ming, Chiu C; Grimaldi, Renato; Gonçalves, Lireny A G; Marsaioli, Anita J

    2016-12-01

    The nutritional and organoleptic attributes of oils can proceed via interesterification of oils blends catalyzed by enzymes or chemicals. Enzymatic interesterification processes are preferred due the regiospecific outcome. Traditionally, monitoring of distribution of fatty acids (FA) in glycerol backbone is performed by enzymatic and chromatographic methods that are time-consuming, involving a series of chemical manipulations employing large volumes of organic solvents. Alternatively, carbon-13 nuclear magnetic resonance ((13)C NMR) is a fast and reliable technique that could be applied to determine the saturated and unsaturated FA distribution of the triacylglycerols (TAGs) present in high oleic sunflower oil (SO) and fully hydrogenated high oleic sunflower oil (HSO) blends and their interesterification products. The enzymatic interesterification was conducted employing the immobilized lipase from Thermomyces lanuginosus (Lipozyme TL IM), the results show that the process was not completely regiospecific at sn-1,3 positions, due to the spontaneous acyl migration from position sn-2 to sn-1,3.

  13. Comparison of the regiospecific distribution from triacylglycerols after chemical and enzymatic interesterification of high oleic sunflower oil and fully hydrogenated high oleic sunflower oil blend by carbon-13 nuclear magnetic resonance.

    Science.gov (United States)

    Lopes, Thiago I B; Ribeiro, Marilene D M M; Ming, Chiu C; Grimaldi, Renato; Gonçalves, Lireny A G; Marsaioli, Anita J

    2016-12-01

    The nutritional and organoleptic attributes of oils can proceed via interesterification of oils blends catalyzed by enzymes or chemicals. Enzymatic interesterification processes are preferred due the regiospecific outcome. Traditionally, monitoring of distribution of fatty acids (FA) in glycerol backbone is performed by enzymatic and chromatographic methods that are time-consuming, involving a series of chemical manipulations employing large volumes of organic solvents. Alternatively, carbon-13 nuclear magnetic resonance ((13)C NMR) is a fast and reliable technique that could be applied to determine the saturated and unsaturated FA distribution of the triacylglycerols (TAGs) present in high oleic sunflower oil (SO) and fully hydrogenated high oleic sunflower oil (HSO) blends and their interesterification products. The enzymatic interesterification was conducted employing the immobilized lipase from Thermomyces lanuginosus (Lipozyme TL IM), the results show that the process was not completely regiospecific at sn-1,3 positions, due to the spontaneous acyl migration from position sn-2 to sn-1,3. PMID:27374579

  14. FT-Raman, FT-IR, UV spectroscopic, NBO and DFT quantum chemical study on the molecular structure, vibrational and electronic transitions of clopidogrel hydrogen sulfate form 1: A comparison to form 2

    Science.gov (United States)

    Srivastava, Anubha; Mishra, Rashmi; Tandon, Poonam; Bansal, A. K.

    2013-03-01

    Clopidogrel hydrogen sulfate (+)-(S)-(2-chlorophenyl)-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-acetate sulfate (1:1), is a selective adenosine diphosphate (ADP) receptor antagonist often used in the treatment of coronary artery, peripheral vascular and cerebrovascular diseases. In the present communication, a comparative study of two polymorphic forms (forms 1 and 2) of clopidogrel hydrogen sulfate (CLP) has been reported. There is difference in conformation and intermolecular hydrogen bonding pattern of two forms. These differences are nicely reflected in the vibrational spectra. The molecular structure, fundamental vibrational frequencies and intensity of the vibrational bands of CLP form 1 are interpreted with the aid of structure optimizations and normal mode analysis based on ab initio HF and DFT method employing 6-311++G(d,p) basis. Polymorphism in CLP have been studied using various characterization tools like FT-Raman, FT-IR spectroscopy and DSC in combination with the quantum chemical calculations. UV-vis spectroscopic studies along with HOMO-LUMO analysis of both polymorphs were performed. The solvent effect calculated by TD-DFT/IEF-PCM/6-31G model results complements with the experimental findings. Stability of the molecule arising from hyper conjugative interactions and charge delocalization has been analyzed using natural bond orbital (NBO) analysis.

  15. Hydrogen economy

    Energy Technology Data Exchange (ETDEWEB)

    Pahwa, P.K.; Pahwa, Gulshan Kumar

    2013-10-01

    In the future, our energy systems will need to be renewable and sustainable, efficient and cost-effective, convenient and safe. Hydrogen has been proposed as the perfect fuel for this future energy system. The availability of a reliable and cost-effective supply, safe and efficient storage, and convenient end use of hydrogen will be essential for a transition to a hydrogen economy. Research is being conducted throughout the world for the development of safe, cost-effective hydrogen production, storage, and end-use technologies that support and foster this transition. This book discusses hydrogen economy vis-a-vis sustainable development. It examines the link between development and energy, prospects of sustainable development, significance of hydrogen energy economy, and provides an authoritative and up-to-date scientific account of hydrogen generation, storage, transportation, and safety.

  16. Modeling of sorption enhanced steam methane reforming—Part II: Simulation within a novel Ca/Cu chemical loop process for hydrogen production

    OpenAIRE

    Fernández García, José Ramón; Abanades García, Juan Carlos; Grasa Adiego, Gemma

    2012-01-01

    The initial stage of a novel Ca/Cu looping process for hydrogen production that involves the sorption enhanced reforming of methane (SER) at high pressure and at a moderate temperature is simulated using a mathematical model developed in Part I of this work. The SER reaction step has been analyzed under dynamic conditions within the framework of the following reactor parameters and operation conditions: catalyst/sorbent ratio, space time, operating temperature, operating pressure and steam/ca...

  17. Electrochemical hydrogen Storage Systems

    International Nuclear Information System (INIS)

    As the global need for energy increases, scientists and engineers have found a possible solution by using hydrogen to power our world. Although hydrogen can be combusted as a fuel, it is considered an energy carrier for use in fuel cells wherein it is consumed (oxidized) without the production of greenhouse gases and produces electrical energy with high efficiency. Chemical storage of hydrogen involves release of hydrogen in a controlled manner from materials in which the hydrogen is covalently bound. Sodium borohydride and aminoborane are two materials given consideration as chemical hydrogen storage materials by the US Department of Energy. A very significant barrier to adoption of these materials as hydrogen carriers is their regeneration from 'spent fuel,' i.e., the material remaining after discharge of hydrogen. The U.S. Department of Energy (DOE) formed a Center of Excellence for Chemical Hydrogen Storage, and this work stems from that project. The DOE has identified boron hydrides as being the main compounds of interest as hydrogen storage materials. The various boron hydrides are then oxidized to release their hydrogen, thereby forming a 'spent fuel' in the form of a lower boron hydride or even a boron oxide. The ultimate goal of this project is to take the oxidized boron hydrides as the spent fuel and hydrogenate them back to their original form so they can be used again as a fuel. Thus this research is essentially a boron hydride recycling project. In this report, research directed at regeneration of sodium borohydride and aminoborane is described. For sodium borohydride, electrochemical reduction of boric acid and sodium metaborate (representing spent fuel) in alkaline, aqueous solution has been investigated. Similarly to literature reports (primarily patents), a variety of cathode materials were tried in these experiments. Additionally, approaches directed at overcoming electrostatic repulsion of borate anion from the cathode, not described in the

  18. Electrochemical hydrogen Storage Systems

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Digby Macdonald

    2010-08-09

    As the global need for energy increases, scientists and engineers have found a possible solution by using hydrogen to power our world. Although hydrogen can be combusted as a fuel, it is considered an energy carrier for use in fuel cells wherein it is consumed (oxidized) without the production of greenhouse gases and produces electrical energy with high efficiency. Chemical storage of hydrogen involves release of hydrogen in a controlled manner from materials in which the hydrogen is covalently bound. Sodium borohydride and aminoborane are two materials given consideration as chemical hydrogen storage materials by the US Department of Energy. A very significant barrier to adoption of these materials as hydrogen carriers is their regeneration from 'spent fuel,' i.e., the material remaining after discharge of hydrogen. The U.S. Department of Energy (DOE) formed a Center of Excellence for Chemical Hydrogen Storage, and this work stems from that project. The DOE has identified boron hydrides as being the main compounds of interest as hydrogen storage materials. The various boron hydrides are then oxidized to release their hydrogen, thereby forming a 'spent fuel' in the form of a lower boron hydride or even a boron oxide. The ultimate goal of this project is to take the oxidized boron hydrides as the spent fuel and hydrogenate them back to their original form so they can be used again as a fuel. Thus this research is essentially a boron hydride recycling project. In this report, research directed at regeneration of sodium borohydride and aminoborane is described. For sodium borohydride, electrochemical reduction of boric acid and sodium metaborate (representing spent fuel) in alkaline, aqueous solution has been investigated. Similarly to literature reports (primarily patents), a variety of cathode materials were tried in these experiments. Additionally, approaches directed at overcoming electrostatic repulsion of borate anion from the cathode, not

  19. Sequential desorption energy of hydrogen from nickel clusters

    Energy Technology Data Exchange (ETDEWEB)

    Deepika,; Kumar, Rakesh, E-mail: rakesh@iitrpr.ac.in [Department of Physics, Indian Institute of Technology Ropar, Rupnagar-140001 (India); R, Kamal Raj. [Indian Institute of Science Education and Research Kolkata, Mohanpur-741246 (India); Kumar, T. J. Dhilip [Department of Chemistry, Indian Institute of Technology Ropar, Rupnagar-140001 (India)

    2015-06-24

    We report reversible Hydrogen adsorption on Nickel clusters, which act as a catalyst for solid state storage of Hydrogen on a substrate. First-principles technique is employed to investigate the maximum number of chemically adsorbed Hydrogen molecules on Nickel cluster. We observe a maximum of four Hydrogen molecules adsorbed per Nickel atom, but the average Hydrogen molecules adsorbed per Nickel atom decrease with cluster size. The dissociative chemisorption energy per Hydrogen molecule and sequential desorption energy per Hydrogen atom on Nickel cluster is found to decrease with number of adsorbed Hydrogen molecules, which on optimization may help in economical storage and regeneration of Hydrogen as a clean energy carrier.

  20. Hydrogen from renewable resources research

    Energy Technology Data Exchange (ETDEWEB)

    Takahashi, P.K.; McKinley, K.R.

    1990-07-01

    In 1986 the Hawaii Natural Energy Institute (HNEI) and the Florida Solar Energy Center (FSEC) were contracted by the Solar Energy Research Institute (SERI) to conduct an assessment of hydrogen production technologies and economic feasibilities of the production and use of hydrogen from renewable resources. In the 1989/90 period all monies were directed toward research and development with an emphasis on integration of tasks, focusing on two important issues, production and storage. The current year's efforts consisted of four tasks, one task containing three subtasks: Hydrogen Production by Gasification of Glucose and Wet Biomass in Supercritical Water; Photoelectrochemical Production of Hydrogen; Photoemission and Photoluminescence Studies of Catalyzed Photoelectrode Surfaces for Hydrogen Production; Solar Energy Chemical Conversion by Means of Photoelectrochemical (PEC) Methods Using Coated Silicon Electrodes; Assessment of Impedance Spectroscopy Methods for Evaluation of Semiconductor-Electrolyte Interfaces; Solar Energy Conversion with Cyanobacteria; Nonclassical Polyhydride Metal Complexes as Hydrogen Storage Materials. 61 refs., 22 figs., 11 tabs.

  1. Hydrogen application dynamics and networks

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, E. [Air Liquide Large Industries, Champigny-sur-Marne (France)

    2010-12-30

    The Chemical Industry consumes large volumes of hydrogen as raw material for the manufacture of numerous products (e.g. polyamides and polyurethanes account for 60% of hydrogen demand). The hydrogen demand was in the recent past and will continue to be driven by the polyurethane family. China will host about 60% of new hydrogen needs over the period 2010-2015 becoming the first hydrogen market next year and reaching 25% of market share by 2015 (vs. only 4% in 2001). Air Liquide supplies large volumes of Hydrogen (and other Industrial Gases) to customers by on-site plants and through pipeline networks which offer significant benefits such as higher safety, reliability and flexibility of supply. Thanks to its long term strategy and heavy investment in large units and pipeline networks, Air Liquide is the Industrial Gas leader in most of the world class Petrochemical basins (Rotterdam, Antwerp, US Gulf Coast, Yosu, Caojing,..) (orig.)

  2. Hydrogen Spectrum

    Science.gov (United States)

    Murdin, P.

    2000-11-01

    The series of absorption or emission lines that are characteristic of the hydrogen atom. According to the Bohr theory of the hydrogen atom, devised by Danish physicist Neils Bohr (1885-1962) in 1913, the hydrogen atom can be envisaged as consisting of a central nucleus (a proton) around which a single electron revolves. The electron is located in one of a number of possible permitted orbits, each...

  3. Predicted Chemical Activation Rate Constants for HO2 + CH2NH: The Dominant Role of a Hydrogen-Bonded Pre-reactive Complex.

    Science.gov (United States)

    Ali, Mohamad Akbar; Sonk, Jason A; Barker, John R

    2016-09-15

    The reaction of methanimine (CH2NH) with the hydroperoxy (HO2) radical has been investigated by using a combination of ab initio and density functional theory (CCSD(T)/CBSB7//B3LYP+Dispersion/CBSB7) and master equation calculations based on transition state theory (TST). Variational TST was used to compute both canonical (CVTST) and microcanonical (μVTST) rate constants for barrierless reactions. The title reaction starts with the reversible formation of a cyclic prereactive complex (PRC) that is bound by ∼11 kcal/mol and contains hydrogen bonds to both nitrogen and oxygen. The reaction path for the entrance channel was investigated by a series of constrained optimizations, which showed that the reaction is barrierless (i.e., no intrinsic energy barrier along the path). However, the variations in the potential energy, vibrational frequencies, and rotational constants reveal that the two hydrogen bonds are formed sequentially, producing two reaction flux bottlenecks (i.e., two transition states) along the reaction path, which were modeled using W. H. Miller's unified TST approach. The rate constant computed for the formation of the PRC is pressure-dependent and increases at lower temperatures. Under atmospheric conditions, the PRC dissociates rapidly and its lifetime is too short for it to undergo significant bimolecular reaction with other species. A small fraction isomerizes via a cyclic transition state and subsequent reactions lead to products normally expected from hydrogen abstraction reactions. The kinetics of the HO2 + CH2NH reaction system differs substantially from the analogous isoelectronic reaction systems involving C2H4 and CH2O, which have been the subjects of previous experimental and theoretical studies.

  4. The influence of chemical surface modification of kenaf fiber using hydrogen peroxide on the mechanical properties of biodegradable kenaf fiber/poly(lactic acid) composites.

    Science.gov (United States)

    Razak, Nur Inani Abdul; Ibrahim, Nor Azowa; Zainuddin, Norhazlin; Rayung, Marwah; Saad, Wan Zuhainis

    2014-01-01

    Bleaching treatment of kenaf fiber was performed in alkaline medium containing hydrogen peroxide solution maintained at pH 11 and 80 °C for 60 min. The bleached kenaf fiber was analyzed using Fourier Transform Infrared (FTIR) and X-ray Diffraction (XRD) analysis. The bleached kenaf fiber was then compounded with poly-(lactic acid) (PLA) via a melt blending method. The mechanical (tensile, flexural and impact) performance of the product was tested. The fiber treatment improved the mechanical properties of PLA/bleached kenaf fiber composites. Scanning electron micrograph (SEM) morphological analysis showed improvement of the interfacial adhesion between the fiber surface and polymer matrix. PMID:24609017

  5. The Influence of Chemical Surface Modification of Kenaf Fiber using Hydrogen Peroxide on the Mechanical Properties of Biodegradable Kenaf Fiber/Poly(Lactic Acid Composites

    Directory of Open Access Journals (Sweden)

    Nur Inani Abdul Razak

    2014-03-01

    Full Text Available Bleaching treatment of kenaf fiber was performed in alkaline medium containing hydrogen peroxide solution maintained at pH 11 and 80 °C for 60 min. The bleached kenaf fiber was analyzed using Fourier Transform Infrared (FTIR and X-ray Diffraction (XRD analysis. The bleached kenaf fiber was then compounded with poly-(lactic acid (PLA via a melt blending method. The mechanical (tensile, flexural and impact performance of the product was tested. The fiber treatment improved the mechanical properties of PLA/bleached kenaf fiber composites. Scanning electron micrograph (SEM morphological analysis showed improvement of the interfacial adhesion between the fiber surface and polymer matrix.

  6. Gamma ray slush hydrogen monitor

    Science.gov (United States)

    Singh, Jag J.; Shen, Chih-Peng; Sprinkle, Danny R.

    1992-01-01

    Mass attenuation for 109Cd radiation have been measured in mixtures of phases and in single phases of five chemical compounds. As anticipated, the mass attenuation coefficients are independent of the phases of the test chemicals. It is recommended that a slush hydrogen monitoring system based on low energy gamma ray attenuation be developed for utilization aboard the NASP.

  7. Chemicals from coal

    Energy Technology Data Exchange (ETDEWEB)

    Harold A. Wittcoff; Bryan G. Reuben; Jeffrey S. Plotkin

    2004-12-01

    This chapter contains sections titled: Chemicals from Coke Oven Distillate; The Fischer-Tropsch Reaction; Coal Hydrogenation; Substitute Natural Gas (SNG); Synthesis Gas Technology; Calcium Carbide; Coal and the Environment; and Notes and References

  8. Chemical functionalization of graphene

    OpenAIRE

    Boukhvalov, D. W.; Katsnelson, M I

    2008-01-01

    Experimental and theoretical results on chemical functionalization of graphene are reviewed. Using hydrogenated graphene as a model system, general principles of the chemical functionalization are formulated and discussed. It is shown that, as a rule, 100% coverage of graphene by complex functional groups (in contrast with hydrogen and fluorine) is unreachable. A possible destruction of graphene nanoribbons by fluorine is considered. The functionalization of infinite graphene and graphene nan...

  9. 化学气相沉积法制备的石墨烯晶畴的氢气刻蚀∗%Hydrogen etching of chemical vap or dep osition-grown graphene domains

    Institute of Scientific and Technical Information of China (English)

    王彬; 冯雅辉; 王秋实; 张伟; 张丽娜; 马晋文; 张浩然; 于广辉; 王桂强

    2016-01-01

    In this paper we analyze the reason of the etching trenches in chemical vapor deposition (CVD) graphene domain and study the influence factor in the distribution and morphology of wrinkles. Graphene is synthesized on Cu substrate. The Cu substrate is annealed at 1050 ◦C for 60 min with 1000 sccm Ar and 200 sccm H2. After annealing, 500 sccm Ar, 20 sccm H2, and 1 sccm dilute CH4 (mixed with Ar) are introduced into the CVD system for graphene growth. Hydrogen etchings of graphene are conducted with flows of 500 sccm Ar and 200 sccm H2 at atmospheric pressure, and etching are performed at 950 and 1050 ◦C. The striated and reticular etching trenches are observed after etching via optical microscope and scanning electron microscope. Every graphene domain is divided into island structures by these etching trenches. However, the edge of graphene domain is not etched and the size of domain is not changed. Electron backscatter diffraction (EBSD) is conducted to analyze the different morphologies of etching trenches. According to the EBSD analysis, the etching trench is closely associated with the Cu crystal orientation. Different Cu planes result in differences in mode, shape, and density of the etching trench. We conduct a verification experiment to judge whether the etching trenches are caused by the gaps between graphene and Cu substrate or by the hydrogenation of wrinkles. The graphene domains grown on Cu substrate with the same growth condition are etched immediately after growth without cooling process. We select graphene which grows across the Cu grain boundary, via optical microscope. A small number of regular hexagons are observed in graphene surface and the region of Cu boundary, but no etching trench is found. As the graphene growing across Cu boundary is the suspending graphene and there is no etching trench, we consider that the gap between graphene and Cu species is not a significant factor of forming etching trench. For comparison, the etching trenches

  10. Chemical energy storage by means of methanol. Silicon fire-technology converts electrolysis hydrogen and carbon dioxide into methanol; Chemische Energiespeicherung mittels Methanol. Silicon-Fire-Technologie wandelt Elektrolysewasserstoff und Kohlendioxid in Methanol um

    Energy Technology Data Exchange (ETDEWEB)

    Meyer-Pittroff, Roland [Technische Univ. Muenchen, Weihenstephan (Germany)

    2012-11-01

    The electric network system will reach its limits due to the further extensive installation of wind and solar power plants. To preserve its operability the generated fluctuating electric energy must be in part transferred into storable energy forms preferably locally. These storable energy carriers can be used economically and ecologically worthwhile mainly outside of the electric network system in other energy consumption sectors like vehicle movement. Accordant the state of technology only the chemical storage can be considered for the needed capacities. During the last years the Silicon Fire-Methanol-Technology has been developed for the synthesis of methanol from electrolysis hydrogen and carbon dioxide coming from concentrated industrial sources. The methanol can be used profitable e.g. as renewable substitute for gasoline or as admixture to gasoline comparable to bio-ethanol - but without competition with foods. (orig.)

  11. Structure and gas-barrier properties of amorphous hydrogenated carbon films deposited on inner walls of cylindrical polyethylene terephthalate by plasma-enhanced chemical vapor deposition

    Science.gov (United States)

    Li, Jing; Gong, Chunzhi; Tian, Xiubo; Yang, Shiqin; Fu, Ricky K. Y.; Chu, Paul K.

    2009-01-01

    The influence of radio-frequency (RF) power on the structure and gas permeation through amorphous hydrogenated carbon films deposited on cylindrical polyethylene terephthalate (PET) samples is investigated. The results show that a higher radio-frequency power leads to a smaller sp 3/sp 2 value but produces fewer defects with smaller size. The permeability of PET samples decreases significantly after a-C:H deposition and the RF only exerts a small influence. However, the coating uniformity, color, and wettability of the surface are affected by the RF power. A higher RF power results in to better uniformity and it may be attributed to the combination of the high-density plasma and sample heating.

  12. Structure and gas-barrier properties of amorphous hydrogenated carbon films deposited on inner walls of cylindrical polyethylene terephthalate by plasma-enhanced chemical vapor deposition

    International Nuclear Information System (INIS)

    The influence of radio-frequency (RF) power on the structure and gas permeation through amorphous hydrogenated carbon films deposited on cylindrical polyethylene terephthalate (PET) samples is investigated. The results show that a higher radio-frequency power leads to a smaller sp3/sp2 value but produces fewer defects with smaller size. The permeability of PET samples decreases significantly after a-C:H deposition and the RF only exerts a small influence. However, the coating uniformity, color, and wettability of the surface are affected by the RF power. A higher RF power results in to better uniformity and it may be attributed to the combination of the high-density plasma and sample heating.

  13. Hydrogen Technology Research at SRNL

    Energy Technology Data Exchange (ETDEWEB)

    Danko, E.

    2011-02-13

    The Savannah River National Laboratory (SRNL) is a U.S. Department of Energy research and development laboratory located at the Savannah River Site (SRS) near Aiken, South Carolina. SRNL has over 50 years of experience in developing and applying hydrogen technology, both through its national defense activities as well as through its recent activities with the DOE Hydrogen Programs. The hydrogen technical staff at SRNL comprises over 90 scientists, engineers and technologists. SRNL has ongoing R&D initiatives in a variety of hydrogen storage areas, including metal hydrides, complex hydrides, chemical hydrides and carbon nanotubes. SRNL has over 25 years of experience in metal hydrides and solid-state hydrogen storage research, development and demonstration. As part of its defense mission at SRS, SRNL developed, designed, demonstrated and provides ongoing technical support for the largest hydrogen processing facility in the world based on the integrated use of metal hydrides for hydrogen storage, separation, and compression. The SRNL has been active in teaming with academic and industrial partners to advance hydrogen technology. A primary focus of SRNL's R&D has been hydrogen storage using metal and complex hydrides. SRNL and its Hydrogen Technology Research Laboratory have been very successful in leveraging their defense infrastructure, capabilities and investments to help solve this country's energy problems. SRNL has participated in projects to convert public transit and utility vehicles for operation using hydrogen fuel. Two major projects include the H2Fuel Bus and an Industrial Fuel Cell Vehicle (IFCV) also known as the GATOR{trademark}. Both of these projects were funded by DOE and cost shared by industry. These are discussed further in Section 3.0, Demonstration Projects. In addition to metal hydrides technology, the SRNL Hydrogen group has done extensive R&D in other hydrogen technologies, including membrane filters for H2 separation, doped carbon

  14. Magnetic liquefier for hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1992-12-31

    This document summarizes work done at the Astronautics Technology Center of the Astronautics Corporation of America (ACA) in Phase 1 of a four phase program leading to the development of a magnetic liquefier for hydrogen. The project involves the design, fabrication, installation, and operation of a hydrogen liquefier providing significantly reduced capital and operating costs, compared to present liquefiers. To achieve this goal, magnetic refrigeration, a recently developed, highly efficient refrigeration technology, will be used for the liquefaction process. Phase 1 project tasks included liquefier conceptual design and analysis, preliminary design of promising configurations, design selection, and detailed design of the selected design. Fabrication drawings and vendor specifications for the selected design were completed during detailed design. The design of a subscale, demonstration magnetic hydrogen liquefier represents a significant advance in liquefaction technology. The cost reductions that can be realized in hydrogen liquefaction in both the subscale and, more importantly, in the full-scale device are expected to have considerable impact on the use of liquid hydrogen in transportation, chemical, and electronic industries. The benefits to the nation from this technological advance will continue to have importance well into the 21st century.

  15. Magnetic liquefier for hydrogen

    International Nuclear Information System (INIS)

    This document summarizes work done at the Astronautics Technology Center of the Astronautics Corporation of America (ACA) in Phase 1 of a four phase program leading to the development of a magnetic liquefier for hydrogen. The project involves the design, fabrication, installation, and operation of a hydrogen liquefier providing significantly reduced capital and operating costs, compared to present liquefiers. To achieve this goal, magnetic refrigeration, a recently developed, highly efficient refrigeration technology, will be used for the liquefaction process. Phase 1 project tasks included liquefier conceptual design and analysis, preliminary design of promising configurations, design selection, and detailed design of the selected design. Fabrication drawings and vendor specifications for the selected design were completed during detailed design. The design of a subscale, demonstration magnetic hydrogen liquefier represents a significant advance in liquefaction technology. The cost reductions that can be realized in hydrogen liquefaction in both the subscale and, more importantly, in the full-scale device are expected to have considerable impact on the use of liquid hydrogen in transportation, chemical, and electronic industries. The benefits to the nation from this technological advance will continue to have importance well into the 21st century

  16. Hydrogen energy progress; Proceedings of the Third World Hydrogen Energy Conference, Tokyo, Japan, June 23-26, 1980. Volumes 1, 2, 3 & 4

    Science.gov (United States)

    Veziroglu, T. N.; Fueki, K.; Ohta, T.

    Papers are presented in the areas of electrolytic hydrogen production, thermochemical and hybrid hydrogen production, innovative hydrogen production, hydrogen storage and transmission, vehicles and hydrogen combustion, chemical and metallurgical usage of hydrogen, overall systems, environmental and materials aspects of hydrogen energy, and industrial aspects of hydrogen energy. Specific topics include advanced alkaline water electrolysis plants, polyethylene-based solid polymer electrolytes, the sulfur-iodine thermochemical water-splitting cycle, hydrogen, carbon monoxide, and char production by flash coal carbonization, photoassisted water electrolysis by Si electrodes, hydrogen production by a thermophilic blue-green alga, the hydrogen storage properties of Fe(1-x)Nb(x)Ti alloys, and hydrogen-fueled compression-ignition engines. Attention is also given to ammonia as an energy vector for the hydrogen economy, a solar hydrogen energy system for an isolated island, a photovoltaic electrolysis system, and the economics of synthetic fuel and chemical production from nuclear power and coal.

  17. California Hydrogen Infrastructure Project

    Energy Technology Data Exchange (ETDEWEB)

    Heydorn, Edward C

    2013-03-12

    Air Products and Chemicals, Inc. has completed a comprehensive, multiyear project to demonstrate a hydrogen infrastructure in California. The specific primary objective of the project was to demonstrate a model of a real-world retail hydrogen infrastructure and acquire sufficient data within the project to assess the feasibility of achieving the nation's hydrogen infrastructure goals. The project helped to advance hydrogen station technology, including the vehicle-to-station fueling interface, through consumer experiences and feedback. By encompassing a variety of fuel cell vehicles, customer profiles and fueling experiences, this project was able to obtain a complete portrait of real market needs. The project also opened its stations to other qualified vehicle providers at the appropriate time to promote widespread use and gain even broader public understanding of a hydrogen infrastructure. The project engaged major energy companies to provide a fueling experience similar to traditional gasoline station sites to foster public acceptance of hydrogen. Work over the course of the project was focused in multiple areas. With respect to the equipment needed, technical design specifications (including both safety and operational considerations) were written, reviewed, and finalized. After finalizing individual equipment designs, complete station designs were started including process flow diagrams and systems safety reviews. Material quotes were obtained, and in some cases, depending on the project status and the lead time, equipment was placed on order and fabrication began. Consideration was given for expected vehicle usage and station capacity, standard features needed, and the ability to upgrade the station at a later date. In parallel with work on the equipment, discussions were started with various vehicle manufacturers to identify vehicle demand (short- and long-term needs). Discussions included identifying potential areas most suited for hydrogen fueling

  18. Florida Hydrogen Initiative

    Energy Technology Data Exchange (ETDEWEB)

    Block, David L

    2013-06-30

    monitoring at any facility engaged in transport, handling and use of hydrogen. Development of High Efficiency Low Cost Electrocatalysts for Hydrogen Production and PEM Fuel Cell Applications ? M. Rodgers, Florida Solar Energy Center The objective of this project was to decrease platinum usage in fuel cells by conducting experiments to improve catalyst activity while lowering platinum loading through pulse electrodeposition. Optimum values of several variables during electrodeposition were selected to achieve the highest electrode performance, which was related to catalyst morphology. Understanding Mechanical and Chemical Durability of Fuel Cell Membrane Electrode Assemblies ? D. Slattery, Florida Solar Energy Center The objective of this project was to increase the knowledge base of the degradation mechanisms for membranes used in proton exchange membrane fuel cells. The results show the addition of ceria (cerium oxide) has given durability improvements by reducing fluoride emissions by an order of magnitude during an accelerated durability test. Production of Low-Cost Hydrogen from Biowaste (HyBrTec?) ? R. Parker, SRT Group, Inc., Miami, FL This project developed a hydrogen bromide (HyBrTec?) process which produces hydrogen bromide from wet-cellulosic waste and co-produces carbon dioxide. Eelectrolysis dissociates hydrogen bromide producing recyclable bromine and hydrogen. A demonstration reactor and electrolysis vessel was designed, built and operated. Development of a Low-Cost and High-Efficiency 500 W Portable PEMFC System ? J. Zheng, Florida State University, H. Chen, Bing Energy, Inc. The objectives of this project were to develop a new catalyst structures comprised of highly conductive buckypaper and Pt catalyst nanoparticles coated on its surface and to demonstrate fuel cell efficiency improvement and durability and cell cost reductions in the buckypaper based electrodes. Development of an Interdisciplinary Hydrogen and Fuel Cell Technology Academic Program ? J

  19. CO2 hydrogenation to methanol

    OpenAIRE

    Frilund, Christian

    2016-01-01

    The literature survey discusses the recent developments in heterogeneous catalytic hydrogenation of CO2 to methanol. Special focus was given to new coated catalysts and reactors. Methanol is an important chemical that is currently produced from synthesis gas. Methanol can also be produced from CO2, but the reaction is less thermodynamically favoured. The main reaction is the exothermic CO2 hydrogenation, and there is a competing fast reaction, the reverse water-gas shift, which converts CO2 t...

  20. Technical Analysis of Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Ali T-Raissi

    2005-01-14

    The aim of this work was to assess issues of cost, and performance associated with the production and storage of hydrogen via following three feedstocks: sub-quality natural gas (SQNG), ammonia (NH{sub 3}), and water. Three technology areas were considered: (1) Hydrogen production utilizing SQNG resources, (2) Hydrogen storage in ammonia and amine-borane complexes for fuel cell applications, and (3) Hydrogen from solar thermochemical cycles for splitting water. This report summarizes our findings with the following objectives: Technoeconomic analysis of the feasibility of the technology areas 1-3; Evaluation of the hydrogen production cost by technology areas 1; and Feasibility of ammonia and/or amine-borane complexes (technology areas 2) as a means of hydrogen storage on-board fuel cell powered vehicles. For each technology area, we reviewed the open literature with respect to the following criteria: process efficiency, cost, safety, and ease of implementation and impact of the latest materials innovations, if any. We employed various process analysis platforms including FactSage chemical equilibrium software and Aspen Technologies AspenPlus and HYSYS chemical process simulation programs for determining the performance of the prospective hydrogen production processes.

  1. Hydrogen. Production and application in industry

    Energy Technology Data Exchange (ETDEWEB)

    Dueker, A. [Sued-Chemie AG, Muenchen (Germany)

    2010-12-30

    Hydrogen is one of the most fascinating elements in Universe. Its unique properties made it to a matter that is used in a wide range of different industrial applications. Besides the chemical role of Hydrogen as a hydrogenation agent, it will play an ever more important role in the global energy house hold. This presentation focuses on the classical technologies for the production of Hydrogen based on a variety of raw materials and will show the most important applications of Hydrogen in large scale industry. (orig.)

  2. Alkenone δD as an ecological indicator: A culture and field study of physiologically-controlled chemical and hydrogen-isotopic variation in C37 alkenones

    Science.gov (United States)

    Wolhowe, Matthew D.; Prahl, Fredrick G.; Langer, Gerald; Oviedo, Angela Maria; Ziveri, Patrizia

    2015-08-01

    A combined culture and field study was conducted in order to (1) more firmly identify the physiological controls on hydrogen isotopic composition of C37 alkenones produced by open-ocean coccolithophores and (2) determine the degree to which these controls are manifested in a natural water column. Nutrient-limitation experiments in culture, combined with previously published data, show that net fractionation between the growth medium and alkenones (αK37) varies with cellular alkenone content and production rate, and, by extension, growth phase. It is hypothesized that the relationship of αK37 with cellular alkenone content and production rate is due to increased use of anabolic NADPH in response to high rates of lipid synthesis. Euphotic zone profiles of δDK37, measured in suspended material from the Gulf of California and Eastern Tropical North Pacific, decreased with depth and light availability, and did not correlate in any expected way with previously-suggested controls on αK37. It is possible that the field data are driven by behavior in light-limited cells that is not represented by the available, nutrient-limited culture data. If true, δDK37 may have utility as an indicator of production depth in settings prone to subsurface production maxima. Relationships between αK37, cell density, and the carbon-isotopic fractionation term εp, however, suggest that αK37 acts an indicator of growth rate, which in this setting is only partially dependent on light, consistent with our interpretation of the culture data. If this latter interpretation proves correct, δDK37 may be a powerful ecological proxy specific to these climatically-important, calcifying, temperature-encoding species.

  3. Room temperature hydrogen gas sensor based on ZnO nanorod arrays grown on a SiO{sub 2}/Si substrate via a microwave-assisted chemical solution method

    Energy Technology Data Exchange (ETDEWEB)

    Hassan, J.J., E-mail: j1j2h72@yahoo.com [Nano-Optoelectronics Research and Technology Laboratory (N.O.R), School of Physics, Universiti Sains Malaysia, Penang 11800 (Malaysia); Department of Physics, College of Science, University of Basrah, Basrah (Iraq); Mahdi, M.A. [Nano-Optoelectronics Research and Technology Laboratory (N.O.R), School of Physics, Universiti Sains Malaysia, Penang 11800 (Malaysia); Department of Physics, College of Science, University of Basrah, Basrah (Iraq); Chin, C.W.; Abu-Hassan, H. [Nano-Optoelectronics Research and Technology Laboratory (N.O.R), School of Physics, Universiti Sains Malaysia, Penang 11800 (Malaysia); Hassan, Z., E-mail: zai@usm.my [Nano-Optoelectronics Research and Technology Laboratory (N.O.R), School of Physics, Universiti Sains Malaysia, Penang 11800 (Malaysia)

    2013-01-05

    Highlights: Black-Right-Pointing-Pointer Highly quality ZnO nanorods arrays were grown on SiO{sub 2} substrate using chemical solution. Black-Right-Pointing-Pointer We use PVA-Zn(OH){sub 2} nanocomposites as seed layer to grow ZnO nanorods. Black-Right-Pointing-Pointer ZnO nanorods arrays show good sensitivity at room temperature to H{sub 2} gas. - Abstract: High-quality zinc oxide (ZnO) nanorod arrays were grown on a silicon dioxide (SiO{sub 2}/Si) substrate via a microwave irradiation-assisted chemical solution method. The SiO{sub 2}/Si substrate was seeded with polyvinyl alcohol-Zn (OH){sub 2} nanocomposites prior to the complete growth of ZnO nanorods through a chemical solution method. X-ray diffraction, field-emission scanning electron microscope, and photoluminescence results indicated the high quality of the produced ZnO nanorods. The hydrogen (H{sub 2})-sensing capabilities of the ZnO nanorod arrays were investigated at room temperature (RT), and the sensitivity was 294% in the presence of 1000 ppm of H{sub 2}. The sensing measurements for H{sub 2} gas at various temperatures (25-250 Degree-Sign C) were repeatable for over 100 min. The sensor exhibited a sensitivity of 1100% at 250 Degree-Sign C upon exposure to 1000 ppm of H{sub 2}. Hysteresis was observed in the sensor at different H{sub 2} concentrations at different temperatures. Moreover, the response times ranged from 60 to 25 s over the range of operating temperatures from RT to 250 Degree-Sign C.

  4. 多孔阳极氧化铝的化学修饰及其应用于过氧化氢的测定%Chemical Modification of Porous Anodic Alumina and Application in Detection of Hydrogen Peroxide

    Institute of Scientific and Technical Information of China (English)

    徐国荣; 唐安平

    2011-01-01

    A new hydrogen peroxide electrochemical biosensor was fabricated through adsorbed cytochrome C in porous anodic alumina chemically modified. The barrier layer at the bottom of the porous anodic alumina was erased by chemical and electrochemical erosion. The Au nano particles were deposited in porous anodic alumina by two-step electroless deposition, and then the cytochrome C was immobilization on Nano Au bed in solution including L-cyste-ine through self-assembled technology. Then a new hydrogen peroxide biosensor was fabricated. The electrochemical and electro catalytic behavior of the cytochrome C electrode was characterized by cyclic voltammetry and chrono-amperometry. The cytochrome C electrode showed a pair of stable and well-defined peaks at about -50 mV and -190 mV at 80 mV/s in pH 7.0 PBS and displayed excellent electro catalytic responses to the reduction of hydrogen peroxide with linear relationship over a concentration range from 1.5xl0-5 mol/L to 4. 8xl0-4 mol/L,and a detection limit of 3.5 x10-6 mol/L( S/N = 3). The results of this study reveal porous anodic alumina chemically modified could be used for the design of biosensors with good operational lifetimes.%多孔阳极氧化铝经化学修饰后吸附细胞色素C,制备了过氧化氢生物传感器电极。多孔阳极氧化铝通过电化学和化学腐蚀阻挡层后,用两步无电沉积方法制备了纳米金修饰的多孔阳极氧化铝电极,再在含有L-半胱氨酸的细胞色素C的溶液中通过吸附制备细胞色素C电极。用循环伏安法和计时电流法测试细胞色素C电极的电化学性能及催化对过氧化氢的还原。结果表明,包覆的细胞色素C电极显示较好的稳定性,在扫描速度为80 mV/s时于-50 mV、-190mV附近出现一对稳定的氧化还原峰。该电极对过氧化氢具有良好的电催化还原性能,在1.5×10-5mol/L~4.8×10-4 mol/L浓度范围内,电流与浓度呈良好的线性关系。多孔阳极氧化铝

  5. Hydrogen program overview

    Energy Technology Data Exchange (ETDEWEB)

    Gronich, S. [Dept. of Energy, Washington, DC (United States). Office of Utility Technologies

    1997-12-31

    This paper consists of viewgraphs which summarize the following: Hydrogen program structure; Goals for hydrogen production research; Goals for hydrogen storage and utilization research; Technology validation; DOE technology validation activities supporting hydrogen pathways; Near-term opportunities for hydrogen; Market for hydrogen; and List of solicitation awards. It is concluded that a full transition toward a hydrogen economy can begin in the next decade.

  6. Photoelectrochemical hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Rocheleau, R.E.; Miller, E.; Zhang, Z. [Univ. of Hawaii, Honolulu, HI (United States)

    1995-09-01

    The large-scale production of hydrogen utilizing energy provided by a renewable source to split water is one of the most ambitious long-term goals of the U.S. Department of Energy`s Hydrogen Program. Photoelectrochemical devices-direct photoconversion systems utilizing a photovoltaic-type structure coated with water-splitting catalysts-represent a promising option to meet this goal. Direct solar-to-chemical conversion efficiencies greater than 7% and photoelectrode lifetimes of up to 30 hours in 1 molar KOH have been demonstrated in our laboratory using low-cost, amorphous-silicon-based photoelectrodes. Loss analysis models indicate that the DOE`s goal of 10% solar-to-chemical conversion can be met with amorphous-silicon-based structures optimized for hydrogen production. In this report, we describe recent progress in the development of thin-film catalytic/protective coatings, improvements in photoelectrode efficiency and stability, and designs for higher efficiency and greater stability.

  7. Hydrogen in metals

    International Nuclear Information System (INIS)

    The report briefly describes the results of the single projects promoted by the German Council of Research (DFG). The subjects deal with diffusion, effusion, permeation and solubility of hydrogen in metals. They are interesting for many disciplines: metallurgy, physical metallurgy, metal physics, materials testing, welding engineering, chemistry, nuclear physics and solid-state physics. The research projects deal with the following interrelated subjects: solubility of H2 in steel and effects on embrittlement, influence of H2 on the fatigue strength of steel as well as the effect of H2 on welded joints. The studies in solid-state research can be divided into methodological and physico-chemical studies. The methodological studies mainly comprise investigations on the analytical determination of H2 by means of nuclear-physical reactions (e.g. the 15N method) and the application of the Moessbauer spectroscopy. Physico-chemical problems are mainly dealt with in studies on interfacial reactions in connection with the absorption of hydrogen and on the diffusion of H2 in different alloy systems. The properties of materials used for hydrogen storage were the subject of several research projects. 20 contributions were separately recorded for the data bank 'Energy'. (MM)

  8. New insights into the interactions between cork chemical components and pesticides. The contribution of π-π interactions, hydrogen bonding and hydrophobic effect.

    Science.gov (United States)

    Olivella, M À; Bazzicalupi, C; Bianchi, A; Fiol, N; Villaescusa, I

    2015-01-01

    The role of chemical components of cork in the sorption of several pesticides has been investigated. For this purpose raw cork and three cork extracted fractions (i.e. cork free of aliphatic extractives, cork free of all extractives and cork free of all extractives and suberin) were used as sorbent of three ionic pesticides (propazine, 2,4-dichlorophenoxy acetic acid (2,4-D) and alachlor) and five non-ionic pesticides (chlorpyrifos, isoproturon, metamitron, methomyl and oxamyl) with a logKow within the range -0.47 to 4.92. The effect of cations on the ionic pesticides, propazine and 2,4-D sorption was also analyzed. Results indicated that the highest yields were obtained for chlorpyrifos and alachlor sorption onto raw cork (>55%). After removal of aliphatic extractives sorption of all pesticides increased that ranged from 3% for propazine to 31% for alachlor. In contrast, removal of phenolic extractives caused a sorption decrease. Low sorption yields were obtained for hydrophobic pesticides such as metamitron, oxamyl and methomyl (cork fractions and extremely low when using raw cork (cork toward aromatic pesticides. Results presented in this paper gain insights into the cork affinities for pesticides and the interactions involved in the sorption process and also enables to envisage sorption affinity of cork for other organic pollutants.

  9. Gold as hydrogen: Structural and electronic properties and chemical bonding in Si3Au3+/0/- and comparisons to Si3H3+/0/-

    Science.gov (United States)

    Kiran, Boggavarapu; Li, Xi; Zhai, Hua-Jin; Wang, Lai-Sheng

    2006-10-01

    A single Au atom has been shown to behave like H in its bonding to Si in several mono- and disilicon gold clusters. In the current work, we investigate the Au /H analogy in trisilicon gold clusters, Si3Au3+/0/-. Photoelectron spectroscopy and density functional calculations are combined to examine the geometric and electronic structure of Si3Au3-. We find that there are three isomers competing for the ground state of Si3Au3- as is the case for Si3H3-. Extensive structural searches show that the potential energy surfaces of the trisilicon gold clusters (Si3Au3-, Si3Au3, and Si3Au3+) are similar to those of the corresponding silicon hydrides. The lowest energy isomers for Si3Au3- and Si3Au3 are structurally similar to a Si3Au four-membered ring serving as a common structural motif. For Si3Au3+, the 2π aromatic cyclotrisilenylium auride ion, analogous to the aromatic cyclotrisilenylium ion (Si3H3+), is the most stable species. Comparison of the structures and chemical bonding between Si3Au3+/0/- and the corresponding silicon hydrides further extends the isolobal analogy between Au and H.

  10. Superconductivity in compressed hydrogen-rich materials: Pressing on hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Struzhkin, Viktor V., E-mail: vstruzhkin@carnegiescience.edu

    2015-07-15

    Highlights: • Anharmonic phonons (quartic anharmonicity) responsible for low T{sub c} in metal hydrides. • Hydrogen-rich group IVA materials are reviewed, SiH{sub 4} and GeH{sub 4}. • Polyhydrides of alkali and alkaline earth metals are shown to have potential for high T{sub c}. • Predictions of room temperature superconductivity in hydrogen and hydrides are critically reviewed. - Abstract: Periodic table of elements starts with hydrogen, a simplest element of all. The simplicity is lost when the element is compressed to high densities or participates in a chemical bonding in compounds, being subjected to “chemical pressure” of surrounding atoms or molecules. The chemical nature of hydrogen is dictated by its simplest electronic shell, which has only one electron. Hydrogen can donate this electron and behave like alkali metal, or accept an extra electron and form a hydride ion with closed shell resembling a group VII element. The complexity of hydrogen goes beyond these simplest configurations, when hydrogen is involved in a multicenter bonding or in hydrogen bonds. This complex behavior is tightly related to the ability of hydrogen to participate in the process of electronic transport in solids and potentially be able to contribute to the superconductivity in a material. Hydrogen by itself when compressed to immense pressures of 400–500 GPa may form a simple atomic phase with very high critical superconducting temperatures (T{sub c}) well above room temperature. While this theoretical insight awaits confirmation at pressures at the limit of current experimental capabilities, a variety of other hydrogen-rich materials have been suggested recently to have record high T{sub c} values. The very existence of many of these materials still lacks experimental confirmation. In this review article, we will present an extensive list of such predicted materials. We will also review superconductivity in classical hydrides (mostly metal hydrides) and current

  11. Solar--hydrogen alternative

    Energy Technology Data Exchange (ETDEWEB)

    1977-03-25

    Solar energy promises more for ecology and a permanent abundant, clean energy source than does the development of atomic energy, with the exception of fusion. And solar methods offer a path for abundant, clean energy which seems far more easily attainable than that of fusion. Wind energy, previosuly regarded as a trivial source, could be used as a massive source of energy if aerogenerators could be located in the high-intensity wind belts of the world where the mean annual wind is more than 25 km/h. Hydrogen could be made from the electricity generated there and be transported to distant points. The availability of massive quantities of hydrogen would give a permanently clean metallurgical and chemical industry.

  12. Metallic Hydrogen

    Science.gov (United States)

    Silvera, Isaac; Zaghoo, Mohamed; Salamat, Ashkan

    2015-03-01

    Hydrogen is the simplest and most abundant element in the Universe. At high pressure it is predicted to transform to a metal with remarkable properties: room temperature superconductivity, a metastable metal at ambient conditions, and a revolutionary rocket propellant. Both theory and experiment have been challenged for almost 80 years to determine its condensed matter phase diagram, in particular the insulator-metal transition. Hydrogen is predicted to dissociate to a liquid atomic metal at multi-megabar pressures and T =0 K, or at megabar pressures and very high temperatures. Thus, its predicted phase diagram has a broad field of liquid metallic hydrogen at high pressure, with temperatures ranging from thousands of degrees to zero Kelvin. In a bench top experiment using static compression in a diamond anvil cell and pulsed laser heating, we have conducted measurements on dense hydrogen in the region of 1.1-1.7 Mbar and up to 2200 K. We observe a first-order phase transition in the liquid phase, as well as sharp changes in optical transmission and reflectivity when this phase is entered. The optical signature is that of a metal. The mapping of the phase line of this transition is in excellent agreement with recent theoretical predictions for the long-sought plasma phase transition to metallic hydrogen. Research supported by the NSF, Grant DMR-1308641, the DOE Stockpile Stewardship Academic Alliance Program, Grant DE-FG52-10NA29656, and NASA Earth and Space Science Fellowship Program, Award NNX14AP17H.

  13. Hydrogen production using plasma processing

    International Nuclear Information System (INIS)

    Plasma processing is a promising method of extracting hydrogen from natural gas while avoiding the greenhouse gas (GHG) production typical of other methods such as steam methane reforming. This presentation describes a plasma discharge process based that, in a single reactor pass, can yield hydrogen concentrations of up to 50 % by volume in the product gas mixture. The process is free of GHG's, does not require catalysts and is easily scalable. Chemical and morphological analyses of the gaseous and solid products of the process by gas-chromatography/mass-spectrometry, microscopic Raman analyses and electron microscopy respectively are reviewed. The direct production of hydrogen-enriched natural gas (HENG) as a fuel for low pollution internal combustion engines and its purification to high-purity hydrogen (99.99%) from the product gas by pressure swing adsorption (PSA) purifier beds are reviewed. The presentation reviews potential commercial applications for the technology

  14. Hydrogen bonding in tight environments

    DEFF Research Database (Denmark)

    Pirrotta, Alessandro; Solomon, Gemma C.; Franco, Ignacio

    2016-01-01

    The single-molecule force spectroscopy of a prototypical class of hydrogen-bonded complexes is computationally investigated. The complexes consist of derivatives of a barbituric acid and a Hamilton receptor that can form up to six simultaneous hydrogen bonds. The force-extension (F-L) isotherms...... of the host-guest complexes are simulated using classical molecular dynamics and the MM3 force field, for which a refined set of hydrogen bond parameters was developed from MP2 ab initio computations. The F-L curves exhibit peaks that signal conformational changes during elongation, the most prominent...... of which is in the 60-180 pN range and corresponds to the force required to break the hydrogen bonds. These peaks in the F-L curves are shown to be sensitive to relatively small changes in the chemical structure of the host molecule. Thermodynamic insights into the supramolecular assembly were obtained...

  15. Saga of hydrogen civilization

    International Nuclear Information System (INIS)

    'Full text': Fossil fuels (i.e., petroleum, natural gas and coal), which meet most of the world's energy demand today, are being depleted quickly. Also, their combustion products are causing global problems such as the greenhouse effect, ozone layer depletion, acid rains and pollution, all of which are posing great danger for our environment and eventually for the life on our planet. Many engineers and scientists agree that the solution to these global problems would be to replace the existing fossil fuel system by the hydrogen energy system. Hydrogen is a very efficient and clean fuel. Its combustion will produce no greenhouse gases, no ozone layer depleting chemicals, and little or no acid rain ingredients and pollution. Hydrogen, produced from renewable energy (e.g., solar) sources, would result in a permanent energy system which we would never have to change. However, there are other energy systems proposed for the post-petroleum era, such as a synthetic fossil fuel system. In this system, synthetic gasoline and synthetic natural gas will be produced using abundant deposits of coal. In a way, this will ensure the continuation of the present fossil fuel system. The two possible energy systems for the post-fossil fuel era (i.e., the solar-hydrogen energy system and the synthetic fossil fuel system) are compared with the present fossil fuel system by taking into consideration production costs, environmental damages and utilization efficiencies. The results indicate that the solar-hydrogen energy system is the best energy system to ascertain a sustainable future, and it should replace the fossil fuel system before the end of the 21st century. (author)

  16. The formation and evolution of hydrogen-deficient post-AGB white dwarfs: the emerging chemical profile and the expectations for the PG1159-DB-DQ evolutionary connection

    CERN Document Server

    Althaus, L G; Panei, J A; Corsico, A H; García-Berro, E; Scoccola, C G

    2005-01-01

    This paper is designed to explore the formation and evolution of hydrogen-deficient post-AGB white dwarfs. To this end, we compute the complete evolution of an initially 2.7 M_sun star from the zero-age main sequence through the thermally pulsing and mass-loss phases to the white dwarf stage. Particular attention is given to the chemical abundance changes during the whole evolution. A time-dependent scheme for the simultaneous treatment of abundance changes caused by nuclear reactions, diffusive overshooting, salt fingers and convection is considered. We employed the double-diffusive mixing-length theory of convection for fluids with composition gradients (Grossman & Taam 1996). The study can therefore be considered as a test of its performance in low-mass stars. Also, time-dependent element diffusion for multicomponent gases is taken into account during the white dwarf evolution. The evolutionary stages corresponding to the last helium thermal pulse on the early white-dwarf cooling branch and the followi...

  17. Hydrogen production processes: an overview

    International Nuclear Information System (INIS)

    Hydrogen, the most abundant element in the universe, does not occur freely on our planet. However, it is predominantly present on earth in combination with oxygen as water and with carbon and other elements as fossil fuels, hydrocarbons, and biomass. Production of hydrogen from these sources is an energy intensive process. Hydrogen production processes can be broadly classified into three general categories: thermal, electrolytic, and photolytic. At present about 96 % of world's hydrogen is produced from fossil fuels using thermal processes like steam methane reforming, partial oxidation, and gasification of coal or biomass while remaining comes from electrolysis of water. Most of the hydrogen produced is primarily used in the chemical industry. More recently hydrogen is perceived as a clean, renewable energy carrier for sustainable energy supply in the future especially when issues like growing concern about global warming due to emission of green house gases and depletion of fossil fuel resources have become paramount. In association with the fuel cell technology, hydrogen appears to be a promising alternative to the fossil fuels for transport applications

  18. Hydrogen and hydrogen isotopes handling experience in heavy water production and related industries

    Energy Technology Data Exchange (ETDEWEB)

    Aprea, J.L. [Argentine Atomic Energy Commission, Comahue Univ., Neuquen (Argentina)

    2002-07-01

    Beyond the conventional applications in the chemical, petrochemical, food and other process industries, hydrogen is also used in nuclear-related industries, where it is required as an active ingredient in large-scale processes to produce heavy water. The experience obtained during the design, construction and operation of such industrial installations, which use hydrogen, deuterium and hydrogen-containing compounds can contribute in favor of the development of safer hydrogen energy facilities. Thus, material selection, properties degradation studies and preventing technologies applied in the heavy water operations are useful tools that will help to overtake the transition towards the hydrogen civilization. (Author)

  19. Decentralized and direct solar hydrogen production: Towards a hydrogen economy in MENA region

    Energy Technology Data Exchange (ETDEWEB)

    Bensebaa, Farid; Khalfallah, Mohamed; Ouchene, Majid

    2010-09-15

    Hydrogen has certainly some advantages in spite of its high cost and low efficiency when compared to other energy vectors. Solar energy is an abundant, clean and renewable source of energy, currently competing with fossil fuel for water heating without subsidy. Photo-electrochemical, thermo-chemicals and photo-biological processes for hydrogen production processes have been demonstrated. These decentralised hydrogen production processes using directly solar energy do not require expensive hydrogen infrastructure for packaging and delivery in the short and medium terms. MENA region could certainly be considered a key area for a new start to a global deployment of hydrogen economy.

  20. Electrochemical Hydrogen Peroxide Generator

    Science.gov (United States)

    Tennakoon, Charles L. K.; Singh, Waheguru; Anderson, Kelvin C.

    2010-01-01

    Two-electron reduction of oxygen to produce hydrogen peroxide is a much researched topic. Most of the work has been done in the production of hydrogen peroxide in basic media, in order to address the needs of the pulp and paper industry. However, peroxides under alkaline conditions show poor stabilities and are not useful in disinfection applications. There is a need to design electrocatalysts that are stable and provide good current and energy efficiencies to produce hydrogen peroxide under acidic conditions. The innovation focuses on the in situ generation of hydrogen peroxide using an electrochemical cell having a gas diffusion electrode as the cathode (electrode connected to the negative pole of the power supply) and a platinized titanium anode. The cathode and anode compartments are separated by a readily available cation-exchange membrane (Nafion 117). The anode compartment is fed with deionized water. Generation of oxygen is the anode reaction. Protons from the anode compartment are transferred across the cation-exchange membrane to the cathode compartment by electrostatic attraction towards the negatively charged electrode. The cathode compartment is fed with oxygen. Here, hydrogen peroxide is generated by the reduction of oxygen. Water may also be generated in the cathode. A small amount of water is also transported across the membrane along with hydrated protons transported across the membrane. Generally, each proton is hydrated with 3-5 molecules. The process is unique because hydrogen peroxide is formed as a high-purity aqueous solution. Since there are no hazardous chemicals or liquids used in the process, the disinfection product can be applied directly to water, before entering a water filtration unit to disinfect the incoming water and to prevent the build up of heterotrophic bacteria, for example, in carbon based filters. The competitive advantages of this process are: 1. No consumable chemicals are needed in the process. The only raw materials

  1. High efficiency stationary hydrogen storage

    Energy Technology Data Exchange (ETDEWEB)

    Hynek, S.; Fuller, W.; Truslow, S. [Arthur D. Little, Inc., Cambridge, MA (United States)

    1995-09-01

    Stationary storage of hydrogen permits one to make hydrogen now and use it later. With stationary hydrogen storage, one can use excess electrical generation capacity to power an electrolyzer, and store the resultant hydrogen for later use or transshipment. One can also use stationary hydrogen as a buffer at fueling stations to accommodate non-steady fueling demand, thus permitting the hydrogen supply system (e.g., methane reformer or electrolyzer) to be sized to meet the average, rather than the peak, demand. We at ADL designed, built, and tested a stationary hydrogen storage device that thermally couples a high-temperature metal hydride to a phase change material (PCM). The PCM captures and stores the heat of the hydriding reaction as its own heat of fusion (that is, it melts), and subsequently returns that heat of fusion (by freezing) to facilitate the dehydriding reaction. A key component of this stationary hydrogen storage device is the metal hydride itself. We used nickel-coated magnesium powder (NCMP) - magnesium particles coated with a thin layer of nickel by means of chemical vapor deposition (CVD). Magnesium hydride can store a higher weight fraction of hydrogen than any other practical metal hydride, and it is less expensive than any other metal hydride. We designed and constructed an experimental NCM/PCM reactor out of 310 stainless steel in the form of a shell-and-tube heat exchanger, with the tube side packed with NCMP and the shell side filled with a eutectic mixture of NaCL, KCl, and MgCl{sub 2}. Our experimental results indicate that with proper attention to limiting thermal losses, our overall efficiency will exceed 90% (DOE goal: >75%) and our overall system cost will be only 33% (DOE goal: <50%) of the value of the delivered hydrogen. It appears that NCMP can be used to purify hydrogen streams and store hydrogen at the same time. These prospects make the NCMP/PCM reactor an attractive component in a reformer-based hydrogen fueling station.

  2. 21 CFR 522.62 - Aminopentamide hydrogen sulfate injection.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Aminopentamide hydrogen sulfate injection. 522.62... § 522.62 Aminopentamide hydrogen sulfate injection. (a) Chemical name. 4-(Dimethylamino)-2,2-diphenylvaleramide hydrogen sulfate. (b) Specifications. It is sterile and each milliliter of aqueous...

  3. Hydrogen-based electrochemical energy storage

    Science.gov (United States)

    Simpson, Lin Jay

    2013-08-06

    An energy storage device (100) providing high storage densities via hydrogen storage. The device (100) includes a counter electrode (110), a storage electrode (130), and an ion conducting membrane (120) positioned between the counter electrode (110) and the storage electrode (130). The counter electrode (110) is formed of one or more materials with an affinity for hydrogen and includes an exchange matrix for elements/materials selected from the non-noble materials that have an affinity for hydrogen. The storage electrode (130) is loaded with hydrogen such as atomic or mono-hydrogen that is adsorbed by a hydrogen storage material such that the hydrogen (132, 134) may be stored with low chemical bonding. The hydrogen storage material is typically formed of a lightweight material such as carbon or boron with a network of passage-ways or intercalants for storing and conducting mono-hydrogen, protons, or the like. The hydrogen storage material may store at least ten percent by weight hydrogen (132, 134) at ambient temperature and pressure.

  4. California Hydrogen Infrastructure Project

    Energy Technology Data Exchange (ETDEWEB)

    Edward C. Heydorn

    2013-03-12

    Air Products and Chemicals, Inc. has completed a comprehensive, multiyear project to demonstrate a hydrogen infrastructure in California. The specific primary objective of the project was to demonstrate a model of a “real-world” retail hydrogen infrastructure and acquire sufficient data within the project to assess the feasibility of achieving the nation’s hydrogen infrastructure goals. The project helped to advance hydrogen station technology, including the vehicle-to-station fueling interface, through consumer experiences and feedback. By encompassing a variety of fuel cell vehicles, customer profiles and fueling experiences, this project was able to obtain a complete portrait of real market needs. The project also opened its stations to other qualified vehicle providers at the appropriate time to promote widespread use and gain even broader public understanding of a hydrogen infrastructure. The project engaged major energy companies to provide a fueling experience similar to traditional gasoline station sites to foster public acceptance of hydrogen. Work over the course of the project was focused in multiple areas. With respect to the equipment needed, technical design specifications (including both safety and operational considerations) were written, reviewed, and finalized. After finalizing individual equipment designs, complete station designs were started including process flow diagrams and systems safety reviews. Material quotes were obtained, and in some cases, depending on the project status and the lead time, equipment was placed on order and fabrication began. Consideration was given for expected vehicle usage and station capacity, standard features needed, and the ability to upgrade the station at a later date. In parallel with work on the equipment, discussions were started with various vehicle manufacturers to

  5. Hydrogen storage: hydrogen as a hydride. 1974-May, 1980 (citations from the NTIS Data Base). Report for 1974-May 80. [135 abstracts

    Energy Technology Data Exchange (ETDEWEB)

    Cavagnaro, D.M.

    1980-06-01

    The bibliography covers hydrogen storage as a hydride. Topics include the chemical and physical properties of the hydride, and how useful it may be for hydrogen storage. Also considered is the conversion of hydrogen to a hydride and the conversion back to hydrogen. (This updated bibliography contains 135 abstracts, 14 of which are new entries to the previous edition.)

  6. HTTR workshop (workshop on hydrogen production technology)

    International Nuclear Information System (INIS)

    Various research and development efforts have been performed to solve the global energy and environmental problems caused by large consumption of fossil fuels. Research activities on advanced hydrogen production technology by the use of nuclear heat from high temperature gas cooled reactors, for example, have been flourished in universities, research institutes and companies in many countries. The Department of HTTR Project and the Department of Advanced Nuclear Heat Technology of JAERI held the HTTR Workshop (Workshop on Hydrogen Production Technology) on July 5 and 6, 2004 to grasp the present status of R and D about the technology of HTGR and the nuclear hydrogen production in the world and to discuss about necessity of the nuclear hydrogen production and technical problems for the future development of the technology. More than 110 participants attended the Workshop including foreign participants from USA, France, Korea, Germany, Canada and United Kingdom. In the Workshop, the presentations were made on such topics as R and D programs for nuclear energy and hydrogen production technologies by thermo-chemical or other processes. Also, the possibility of the nuclear hydrogen production in the future society was discussed. The workshop showed that the R and D for the hydrogen production by the thermo-chemical process has been performed in many countries. The workshop affirmed that nuclear hydrogen production could be one of the competitive supplier of hydrogen in the future. The second HTTR Workshop will be held in the autumn next year. (author)

  7. Hydrogen storage in nanostructured materials

    Energy Technology Data Exchange (ETDEWEB)

    Assfour, Bassem

    2011-02-28

    Hydrogen is an appealing energy carrier for clean energy use. However, storage of hydrogen is still the main bottleneck for the realization of an energy economy based on hydrogen. Many materials with outstanding properties have been synthesized with the aim to store enough amount of hydrogen under ambient conditions. Such efforts need guidance from material science, which includes predictive theoretical tools. Carbon nanotubes were considered as promising candidates for hydrogen storage applications, but later on it was found to be unable to store enough amounts of hydrogen under ambient conditions. New arrangements of carbon nanotubes were constructed and hydrogen sorption properties were investigated using state-of-the-art simulation methods. The simulations indicate outstanding total hydrogen uptake (up to 19.0 wt.% at 77 K and 5.52wt.% at 300 K), which makes these materials excellent candidates for storage applications. This reopens the carbon route to superior materials for a hydrogen-based economy. Zeolite imidazolate frameworks are subclass of MOFs with an exceptional chemical and thermal stability. The hydrogen adsorption in ZIFs was investigated as a function of network geometry and organic linker exchange. Ab initio calculations performed at the MP2 level to obtain correct interaction energies between hydrogen molecules and the ZIF framework. Subsequently, GCMC simulations are carried out to obtain the hydrogen uptake of ZIFs at different thermodynamic conditions. The best of these materials (ZIF-8) is found to be able to store up to 5 wt.% at 77 K and high pressure. We expected possible improvement of hydrogen capacity of ZIFs by substituting the metal atom (Zn{sup 2+}) in the structure by lighter elements such as B or Li. Therefore, we investigated the energy landscape of LiB(IM)4 polymorphs in detail and analyzed their hydrogen storage capacities. The structure with the fau topology was shown to be one of the best materials for hydrogen storage. Its

  8. Estimation of optimal capacity of the module through the demand analysis of refinery hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Young-Seek; Kim, Ho-Jin; Kim, Il-Su [SK energy Institution of Technology, Daejeon (Korea, Republic of)] (and others)

    2006-02-15

    Hydrogen is focused as energy carrier, not an energy source on the rising of problems such as exhaustion of fossil fuel and environment pollution. Thermochemical hydrogen production by nuclear energy has potential to efficiently produce large quantities of hydrogen without producing greenhouse gases. The oil refiners and petro-chemical plant are very large, centralized producers and users of industrial hydrogen, and they a high-potential early market for hydrogen produced by nuclear energy. Therefore, hydrogen market of petro-chemical industry as demand site for nuclear hydrogen was investigated and worked for demand forecast of hydrogen in 2020. Also we suggested possible supply plans of nuclear hydrogen considered regional characteristics. The hydrogen production cost was analyzed and estimated for nuclear hydrogen as well as conventional hydrogen production such as natural gas reforming and coal gasification in various range.

  9. Selective production of hydrogen peroxide and oxidation of hydrogen sulfide in an unbiased solar photoelectrochemical cell

    DEFF Research Database (Denmark)

    Zong, Xu; Chen, Hongjun; Seger, Brian;

    2014-01-01

    A solar-to-chemical conversion process is demonstrated using a photoelectrochemical cell without external bias for selective oxidation of hydrogen sulfide (H2S) to produce hydrogen peroxide (H2O2) and sulfur (S). The process integrates two redox couples anthraquinone/anthrahydroquinone and I−/I3...

  10. Steam reforming of sunflower oil for hydrogen gas production

    OpenAIRE

    Dupont V.

    2007-01-01

    Methods of current hydrogen production for the petroleum refinery industry as well as future technologies under research and development in preparation for a global hydrogen-based economy are briefly reviewed. The advantages of biomass and of liquid biofuels, including vegetable oils as fuel sources in the sustainable production of hydrogen gas are then presented. The bulk of this lecture is thereafter concerned with the thermo-chemical means of hydrogen production which are suitable to the c...

  11. INVESTIGATIONS ON BIOCHEMICAL PURIFICATION OF GROUND WATER FROM HYDROGEN SULFIDE

    OpenAIRE

    Yu. P. Sedlukho; Yu. O. Stankevich

    2015-01-01

    The paper considers problems and features of biochemical removal of hydrogen sulfide from ground water. The analysis of existing methods for purification of ground water from hydrogen sulfide has been given in the paper. The paper has established shortcomings of physical and chemical purification of ground water. While using aeration methods for removal of hydrogen sulfide formation of colloidal sulfur that gives muddiness and opalescence to water occurs due to partial chemical air oxidation....

  12. Hydrogen Education Curriculum Path at Michigan Technological University

    Energy Technology Data Exchange (ETDEWEB)

    Keith, Jason; Crowl, Daniel; Caspary, David; Naber, Jeff; Allen, Jeff; Mukerjee, Abhijit; Meng, Desheng; Lukowski, John; Solomon, Barry; Meldrum, Jay

    2012-01-03

    The objective of this project was four-fold. First, we developed new courses in alternative energy and hydrogen laboratory and update existing courses in fuel cells. Secondly, we developed hydrogen technology degree programs. Thirdly, we developed hydrogen technology related course material for core courses in chemical engineering, mechanical engineering, and electrical engineering. Finally, we developed fuel cell subject material to supplement the Felder & Rousseau and the Geankoplis chemical engineering undergraduate textbooks.

  13. Polarographic catalytic wave of hydrogen--Parallel catalytic hydrogen wave of bovine serum albumin in thepresence of oxidants

    Institute of Scientific and Technical Information of China (English)

    GUO; Wei(过玮); LIU; Limin(刘利民); LIN; Hong(林洪); SONG; Junfeng(宋俊峰)

    2002-01-01

    A polarographic catalytic hydrogen wave of bovine serum albumin (BSA) at about -1.80 V (vs. SCE) in NH4Cl-NH3@H2O buffer is further catalyzed by such oxidants as iodate, persulfate and hydrogen peroxide, producing a kinetic wave. Studies show that the kinetic wave is a parallel catalytic wave of hydrogen, which resulted from that hydrogen ion is electrochemically reduced and chemically regenerated through oxidation of its reduction product, atomic hydrogen, by oxidants mentioned above. It is a new type of poralographic catalytic wave of protein, which is suggested to be named as a parallel catalytic hydrogen wave.

  14. Nuclear energy for sustainable Hydrogen production

    International Nuclear Information System (INIS)

    There is general agreement that hydrogen as an universal energy carrier could play increasingly important role in energy future as part of a set of solutions to a variety of energy and environmental problems. Given its abundant nature, hydrogen has been an important raw material in the organic chemical industry. At recent years strong competition has emerged between nations as diverse as the U.S., Japan, Germany, China and Iceland in the race to commercialize hydrogen energy vehicles in the beginning of 21st Century. Any form of energy - fossil, renewable or nuclear - can be used to generate hydrogen. The hydrogen production by nuclear electricity is considered as a sustainable method. By our presentation we are trying to evaluate possibilities for sustainable hydrogen production by nuclear energy at near, medium and long term on EC strategic documents basis. The main EC documents enter water electrolysis by nuclear electricity as only sustainable technology for hydrogen production in early stage of hydrogen economy. In long term as sustainable method is considered the splitting of water by thermochemical technology using heat from high temperature reactors too. We consider that at medium stage of hydrogen economy it is possible to optimize the sustainable hydrogen production by high temperature and high pressure water electrolysis by using a nuclear-solar energy system. (author)

  15. A review of experimental studies of hydrogen as a new therapeutic agent in emergency and critical care medicine

    OpenAIRE

    Shen, Meihua; Zhang, Hongying; Yu, Congjun; Wang, Fan; Sun, Xuejun

    2014-01-01

    Hydrogen is the most abundant chemical element in the Universe, but is seldom regarded as a therapeutic agent. Recent evidence has shown that hydrogen is a potent antioxidative, antiapoptotic and anti-inflammatory agent and so may have potential medical applications in cells, tissues and organs. There are several methods to administer hydrogen, such as inhalation of hydrogen gas, aerosol inhalation of a hydrogen-rich solution, drinking hydrogen dissolved in water, injecting hydrogen-rich sali...

  16. Hydrogen-based industry from remote excess hydroelectricity

    International Nuclear Information System (INIS)

    This paper examines synergies, opportunities and barriers associated with hydrogen and excess hydro-electricity in remote areas. The work is based on a case study that examined the techno-economic feasibility of a new hydrogen-based industry using surplus/off-peak generating capacity of the Taltson Dam and Generating Station in the Northwest Territories, Canada. After evaluating the amount and cost of hydrogen that could be produced from the excess capacity, the study investigates three hydrogen utilization scenarios: (1) merchant liquid or compressed hydrogen, (2) hydrogen as a chemical feedstock for the production of hydrogen peroxide, (3) methanol production from biomass, oxygen and hydrogen. Hydrogen peroxide production is the most promising and attractive strategy in the Fort Smith context. The study also illustrates patterns that recur in isolated sites throughout the world. (Author)

  17. Hydrogen Storage and Production Project

    Energy Technology Data Exchange (ETDEWEB)

    Bhattacharyya, Abhijit [Univ. of Arkansas, Little Rock, AR (United States); Biris, A. S. [Univ. of Arkansas, Little Rock, AR (United States); Mazumder, M. K. [Univ. of Arkansas, Little Rock, AR (United States); Karabacak, T. [Univ. of Arkansas, Little Rock, AR (United States); Kannarpady, Ganesh [Univ. of Arkansas, Little Rock, AR (United States); Sharma, R. [Univ. of Arkansas, Little Rock, AR (United States)

    2011-07-31

    This is the final technical report. This report is a summary of the project. The goal of our project is to improve solar-to-hydrogen generation efficiency of the PhotoElectroChemical (PEC) conversion process by developing photoanodes with high absorption efficiency in the visible region of the solar radiation spectrum and to increase photo-corrosion resistance of the electrode for generating hydrogen from water. To meet this goal, we synthesized nanostructured heterogeneous semiconducting photoanodes with a higher light absorption efficiency compared to that of TiO2 and used a corrosion protective layer of TiO2. While the advantages of photoelectrochemical (PEC) production of hydrogen have not yet been realized, the recent developments show emergence of new nanostructural designs of photoanodes and choices of materials with significant gains in photoconversion efficiency.

  18. Hydrogen storage by physisorption on porous materials

    Energy Technology Data Exchange (ETDEWEB)

    Panella, B.

    2006-09-13

    A great challenge for commercializing hydrogen powered vehicles is on-board hydrogen storage using economic and secure systems. A possible solution is hydrogen storage in light-weight solid materials. Here three principle storage mechanisms can be distinguished: i) absorption of hydrogen in metals ii) formation of compounds with ionic character, like complex hydrides and iii) physisorption (or physical adsorption) of hydrogen molecules on porous materials. Physical adsorption exhibits several advantages over chemical hydrogen storage as for example the complete reversibility and the fast kinetics. Two classes of porous materials were investigated for physical hydrogen storage, i.e. different carbon nanostructures and crystalline metal-organic frameworks possessing extremely high specific surface area. Hydrogen adsorption isotherms were measured using a Sieverts' apparatus both at room temperature and at 77 K at pressures up to the saturation regime. Additionally, the adsorption sites of hydrogen in these porous materials were identified using thermal desorption spectroscopy extended to very low temperatures (down to 20 K). Furthermore, the adsorbed hydrogen phase was studied in various materials using Raman spectroscopy at different pressures and temperatures. The results show that the maximum hydrogen storage capacity of porous materials correlates linearly with the specific surface area and is independent of structure and composition. In addition the pore structure of the adsorbent plays an important role for hydrogen storage since the adsorption sites for H2 could be assigned to pores possessing different dimensions. Accordingly it was shown that small pores are necessary to reach high storage capacities already at low pressures. This new understanding may help to tailor and optimize new porous materials for hydrogen storage. (orig.)

  19. Cutaneous reactions simulating erythema multiforme and Stevens Johnson syndrome due to occupational exposure to a plant-growth regulator

    Directory of Open Access Journals (Sweden)

    Inamadar Arun

    2007-01-01

    Full Text Available Background: In India, hydrogen cyanamide (Dormex ® is a plant growth regulator used mainly for the bud-breaking of grapevines. The use of this chemical may result in severe cutaneous reactions simulating erythema multiforme (EM, Stevens-Johnson syndrome (SJS and toxic epidermal necrolysis (TEN. Methods: Studies were conducted on four seasonal grapevine workers who developed severe cutaneous reactions following the unprotected use of Dormex ® (hydrogen cyanamide. Results: Two of the patients had EM-like skin lesions and the other two developed SJS-TEN-like skin lesions. A latent period of 5-7 days existed between the contact with the chemical and the development of the skin lesions. The histopathological picture was suggestive of EM. All the patients responded to systemic steroids and antihistamines. Conclusions: Hydrogen cyanamide may act as a hapten, initiating cytotoxic immunological attack on keratinocytes, resulting in EM- and SJS-TEN-like clinical picture. Awareness regarding such severe cutaneous reactions due to the inappropriate handling of Dormex ® is required. The use of personal protection equipments while handling agricultural chemicals is essential.

  20. Hydrogen production processes

    International Nuclear Information System (INIS)

    The goals of this first Gedepeon workshop on hydrogen production processes are: to stimulate the information exchange about research programs and research advances in the domain of hydrogen production processes, to indicate the domains of interest of these processes and the potentialities linked with the coupling of a nuclear reactor, to establish the actions of common interest for the CEA, the CNRS, and eventually EDF, that can be funded in the framework of the Gedepeon research group. This document gathers the slides of the 17 presentations given at this workshop and dealing with: the H2 question and the international research programs (Lucchese P.); the CEA's research program (Lucchese P., Anzieu P.); processes based on the iodine/sulfur cycle: efficiency of a facility - flow-sheets, efficiencies, hard points (Borgard J.M.), R and D about the I/S cycle: Bunsen reaction (Colette S.), R and D about the I/S cycle: the HI/I2/H2O system (Doizi D.), demonstration loop/chemical engineering (Duhamet J.), materials and corrosion (Terlain A.); other processes under study: the Westinghouse cycle (Eysseric C.), other processes under study at the CEA (UT3, plasma,...) (Lemort F.), database about thermochemical cycles (Abanades S.), Zn/ZnO cycle (Broust F.), H2 production by cracking, high temperature reforming with carbon trapping (Flamant G.), membrane technology (De Lamare J.); high-temperature electrolysis: SOFC used as electrolyzers (Grastien R.); generic aspects linked with hydrogen production: technical-economical evaluation of processes (Werkoff F.), thermodynamic tools (Neveu P.), the reactor-process coupling (Aujollet P.). (J.S.)

  1. Tribology in Gaseous Hydrogen

    Science.gov (United States)

    Sawae, Yoshinori; Sugimura, Joich

    Hydrogen is expected as a clean and renewable energy carrier for future environment-friendly society. Many machine elements in hydrogen energy systems should be operating within hydrogen gas and tribological behavior, such as friction and wear, of bearings and seals are affected by the hydrogen environment through some interactions between material surfaces and gaseous hydrogen, i.e., physisorption of hydrogen molecules and following chemisorptions of dissociated atoms on metal surfaces, formation of metal hydride and reduction of metal oxide layer by hydrogen atoms diffused into bulk. Therefore, friction and wear characteristics of tribomaterials in the hydrogen environment should be appropriately understood to establish a design guideline for reliable hydrogen utilizing systems. This paper reviews the current knowledge about the effect of hydrogen on friction and wear of materials, and then describes our recent progress of hydrogen research in the tribology field.

  2. Hydrogen in aluminum during alkaline corrosion

    Energy Technology Data Exchange (ETDEWEB)

    Adhikari, Saikat; Ai, Jiahe [Department of Chemical and Biological Engineering, Iowa State University, Ames, IA 50011 (United States); Hebert, Kurt R., E-mail: krhebert@iastate.ed [Department of Chemical and Biological Engineering, Iowa State University, Ames, IA 50011 (United States); Ho, K.M.; Wang, C.Z. [US DOE, Ames Laboratory, Ames, IA 50011 (United States)] [Department of Physics and Astronomy, Iowa State University, Ames, IA 50011 (United States)

    2010-07-30

    The thermodynamic state of hydrogen in aluminum during alkaline corrosion was investigated, using a two-compartment hydrogen permeation cell with an Al/Pd bilayer membrane. The open-circuit potential of the Pd layer in a pH 7.0 buffer solution was monitored to sense the hydrogen chemical potential, {mu}{sub H}. At pH 12.5-13.5, the measurements established a minimum {mu}{sub H} of 0.55 eV relative to the ideal gas reference, equivalent to a H{sub 2} gas pressure of 5.7 GPa. Statistical mechanics calculations show that vacancy-hydrogen defects are stable in Al at this condition. A dissolution mechanism was proposed in which H at very high {mu}{sub H} is produced by oxidation of interfacial aluminum hydride. The mechanism explains the observed rapid accumulation of H in the metal by extensive formation of vacancy-hydrogen defects.

  3. Alloying effect on the electronic structures of hydrogen storage compounds

    Energy Technology Data Exchange (ETDEWEB)

    Yukawa, H.; Moringa, M.; Takahashi, Y. [Nagoya Univ. (Japan). Dept. of Mater. Sci. and Eng.

    1997-05-20

    The electronic structures of hydrogenated LaNi{sub 5} containing various 3d transition elements were investigated by the DV-X{alpha} molecular orbital method. The hydrogen atom was found to form a strong chemical bond with the Ni rather than the La atoms. The alloying modified the chemical bond strengths between atoms in a small metal octahedron containing a hydrogen atom at the center, resulting in the change in the hydrogen absorption and desorption characteristics of LaNi{sub 5} with alloying. (orig.) 7 refs.

  4. A hydrogen ice cube

    NARCIS (Netherlands)

    Schrauwers, A.

    2004-01-01

    Hydrogen is considered to be a highly promising energy carrier. Nonetheless, before hydrogen can become the fuel of choice for the future a number of slight problems will have to be overcome. For example, how can hydrogen be safely stored? Motor vehicles running on hydrogen may be clean in concept b

  5. LIGHT-WEIGHT NANOCRYSTALLINE HYDROGEN STORAGE MATERIALS

    Energy Technology Data Exchange (ETDEWEB)

    S. G. Sankar; B. Zande; R.T. Obermyer; S. Simizu

    2005-11-21

    During Phase I of this SBIR Program, Advanced Materials Corporation has addressed two key issues concerning hydrogen storage: 1. We have conducted preliminary studies on the effect of certain catalysts in modifying the hydrogen absorption characteristics of nanocrystalline magnesium. 2. We have also conducted proof-of-concept design and construction of a prototype instrument that would rapidly screen materials for hydrogen storage employing chemical combinatorial technique in combination with a Pressure-Composition Isotherm Measurement (PCI) instrument. 3. Preliminary results obtained in this study approach are described in this report.

  6. Hydrogen: an energy vector for the future?

    Energy Technology Data Exchange (ETDEWEB)

    His, St

    2004-07-01

    Used today in various industrial sectors including refining and chemicals, hydrogen is often presented as a promising energy vector for the transport sector. However, its balance sheet presents disadvantages as well as advantages. For instance, some of its physical characteristics are not very well adapted to transport use and hydrogen does not exist in pure form. Hydrogen technologies can offer satisfactory environmental performance in certain respects, but remain handicapped by costs too high for large-scale development. A great deal of research will be required to develop mass transport application. (author)

  7. Hydrogen energy - An inexhaustible abundant clean energy system

    Science.gov (United States)

    Nayar, M. G.

    1981-04-01

    A review is presented of various hydrogen production processes from possible primary energy resources. The processes covered are nuclear coal gasification, thermochemical hydrogen production, and hydrogen production by electrolysis, which includes solid polymer electrolyte-based electrolyzers, high-temperature electrolyzers, and photoelectrochemical decomposition of water. Attention is given to hydrogen transport and storage (in metal hydride systems) and to its application as an automotive fuel. Hydrogen as a secondary energy source is also discussed, and its uses as an off-peak power storage medium and as an energy transmission medium are described. Costs, flow diagrams and chemical formulas are analyzed in detail.

  8. Alloying effects on hydrogen permeability of V without catalytic Pd overlayer

    Energy Technology Data Exchange (ETDEWEB)

    Nakamura, Y.; Yukawa, H.; Suzuki, A. [Department of Materials Science and Engineering, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8603 (Japan); Nambu, T. [Department of Materials Science and Engineering, Suzuka National College of Technology, Shiroko-cho, Suzuka, Mie 510-0294 (Japan); Matsumoto, Y. [Department of Mechanical Engineering, Oita National College of Technology, Maki, Oita 870-0152 (Japan); Murata, Y. [Department of Materials Science and Engineering, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8603 (Japan)

    2015-10-05

    Highlights: • Air–treated V–based alloy membranes without catalytic Pd overlayer are found to possess excellent hydrogen permeability. • They also exhibit good durability at high temperature. • Alloying effects are discussed in view of the new description of hydrogen permeation based on hydrogen chemical potential. - Abstract: Hydrogen permeability of air–treated V–based alloy membranes without Pd coating have been investigated. The diffusion–limiting hydrogen permeation reaction takes place even without catalytic Pd overlayer on the surface. It is shown that pure V and its alloy membranes without Pd overlayer possess excellent hydrogen permeability and good durability at high temperature. The new description of hydrogen permeation based on hydrogen chemical potential has been applied and the hydrogen flux is analyzed in terms of the mobility of hydrogen atom and the PCT factor, f{sub PCT}.

  9. 过氧化氢抛光液体系中钌的化学机械抛光研究%Chemical Mechanical Planarization of Ruthenium in Hydrogen Peroxide- Based Slurry

    Institute of Scientific and Technical Information of China (English)

    储向峰; 王婕; 董永平; 乔红斌; 张王兵

    2012-01-01

    本文研究了过氧化氢(H2O2)抛光液体系中金属钌的化学机械抛光行为,采用电化学分析方法和X射线光电子能谱仪(XPS)分析了氧化剂和络合剂对腐蚀效果的影响,利用原子力显微镜(AFM)观察抛光表面的微观形貌.结果表明:在过氧化氢抛光液体系中,金属钌表面钝化膜的致密度和厚度与醋酸(CH3COOH)和H2O2的浓度有关.抛光液中醋酸主要通过促进阳极反应的进行从而增强抛光液对金属钌的化学作用,CH3COOH作为络合剂比三乙醇胺(TEA)或酒石酸(C4H6O6)得到的抛光速率更高.低浓度H2O2通过增强抛光液对金属钌的化学腐蚀,抛光速率增大,较高浓度H2O2可能通过在金属表面形成较厚的氧化膜,抛光速率下降.XPS图谱说明钌片浸泡在含醋酸介质过氧化氢体系抛光液后,钌、氧原子相对含量之比约为2∶3,而且金属钌被氧化到四价和八价,这可能是因为金属钌表面生成RuO2和RuO4.抛光后的金属钌表面在5μm×5μm范围内平均粗糙度Sa由抛光前的33 nm降至6.99 nm.%In this paper,chemical mechanical polishing behaviors of Ruthenium(Ru) in hydrogen peroxide(H2O2)-based slurry are investigated.The effect of the oxidizing agent and complexing agents on the corrosion behaviors are investigated by using electrochemical measurement and X-ray photoelectron spectroscopy.And the polished Ru surface is characterized by atomic force microscopy.Results show that the tightness and thickness of the passive film on the surface of Ru are related to the concentrations of CH3COOH and H2O2.CH3COOH can accelerate the anode reaction and enhance the chemical action of the slurry on the surface of Ru.The material removal rate(MRR) of Ru in slurries with CH3COOH as complexing agent is higher than that of TEA or C4H6O6.H2O2 at low concentration promotes the chemical corrosion ability to corrode Ru surface and increases MRR,the increasing of H2O2 concentration may

  10. Hydrogen-related effects in crystalline semiconductors

    International Nuclear Information System (INIS)

    Recent experimental and theoretical information regarding the states of hydrogen in crystalline semiconductors is reviewed. The abundance of results illustrates that hydrogen does not preferentially occupy a few specific lattice sites but that it binds to native defects and impurities, forming a large variety of neutral and electrically active complexes. The study of hydrogen passivated shallow acceptors and donors and of partially passivated multivalent acceptors has yielded information on the electronic and real space structure and on the chemical composition of these complexes. Infrared spectroscopy, ion channeling, hydrogen isotope substitution and electric field drift experiments have shown that both static trigonal complexes as well as centers with tunneling hydrogen exist. Total energy calculations indicate that the charge state of the hydrogen ion which leads to passivation dominates, i.e., H+ in p-type and H/sup /minus// in n-type crystals. Recent theoretical calculations indicate that is unlikely for a large fraction of the atomic hydrogen to exist in its neutral state, a result which is consistent with the total absence of any Electron Paramagnetic Resonance (EPR) signal. An alternative explanation for this result is the formation of H2. Despite the numerous experimental and theoretical results on hydrogen-related effects in Ge and Si there remains a wealth of interesting physics to be explored, especially in compound and alloy semiconductors. 6 refs., 6 figs

  11. Detection of hydrogen peroxide with chemiluminescent micelles

    Directory of Open Access Journals (Sweden)

    Dongwon Lee

    2008-08-01

    Full Text Available Dongwon Lee1, Venkata R Erigala1,3, Madhuri Dasari1, Junhua Yu2, Robert M Dickson2, Niren Murthy11The Wallace H. Coulter Department of Biomedical Engineering; 2Department of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA, USA; 3The Scripps Research Institute, La Jolla, CA, USAAbstract: The overproduction of hydrogen peroxide is implicated in the progress of numerous life-threatening diseases and there is a great need for the development of contrast agents that can detect hydrogen peroxide in vivo. In this communication, we present a new contrast agent for hydrogen peroxide, termed peroxalate micelles, which detect hydrogen peroxide through chemiluminescence, and have the physical/chemical properties needed for in vivo imaging applications. The peroxalate micelles are composed of amphiphilic peroxalate based copolymers and the fluorescent dye rubrene, they have a ‘stealth’ polyethylene glycol (PEG corona to evade macrophage phagocytosis, and a diameter of 33 nm to enhance extravasation into permeable tissues. The peroxalate micelles can detect nanomolar concentrations of hydrogen peroxide (>50 nM and thus have the sensitivity needed to detect physiological concentrations of hydrogen peroxide. We anticipate numerous applications of the peroxalate micelles for in vivo imaging of hydrogen peroxide, given their high sensitivity, small size, and biocompatible PEG corona.Keywords: hydrogen peroixde, chemiluminescence, micelles, amphiphilic copolymer

  12. Hydrogen local vibrational modes in semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    McCluskey, M D [Univ. of California, Berkeley, CA (United States). Dept. of Physics

    1997-06-01

    Following, a review of experimental techniques, theory, and previous work, the results of local vibrational mode (LVM) spectroscopy on hydrogen-related complexes in several different semiconductors are discussed. Hydrogen is introduced either by annealing in a hydrogen ambient. exposure to a hydrogen plasma, or during growth. The hydrogen passivates donors and acceptors in semiconductors, forming neutral complexes. When deuterium is substituted for hydrogen. the frequency of the LVM decreases by approximately the square root of two. By varying the temperature and pressure of the samples, the microscopic structures of hydrogen-related complexes are determined. For group II acceptor-hydrogen complexes in GaAs, InP, and GaP, hydrogen binds to the host anion in a bond-centered orientation, along the [111] direction, adjacent to the acceptor. The temperature dependent shift of the LVMs are proportional to the lattice thermal energy U(T), a consequence of anharmonic coupling between the LVM and acoustical phonons. In the wide band gap semiconductor ZnSe, epilayers grown by metalorganic chemical vapor phase epitaxy (MOCVD) and doped with As form As-H complexes. The hydrogen assumes a bond-centered orientation, adjacent to a host Zn. In AlSb, the DX centers Se and Te are passivated by hydrogen. The second, third, and fourth harmonics of the wag modes are observed. Although the Se-D complex has only one stretch mode, the Se-H stretch mode splits into three peaks. The anomalous splitting is explained by a new interaction between the stretch LVM and multi-phonon modes of the lattice. As the temperature or pressure is varied, and anti-crossing is observed between LVM and phonon modes.

  13. Why hydrogen; Pourquoi l'hydrogene?

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2004-02-01

    The energy consumption increase and the associated environmental risks, led to develop new energy sources. The authors present the potentialities of the hydrogen in this context of energy supply safety. They detail the today market and the perspectives, the energy sources for the hydrogen production (fossils, nuclear and renewable), the hydrogen transport, storage, distribution and conversion, the application domains, the associated risks. (A.L.B.)

  14. Hydrogen bonded supramolecular structures

    CERN Document Server

    Li, Zhanting

    2015-01-01

    This book covers the advances in the studies of hydrogen-bonding-driven supramolecular systems  made over the past decade. It is divided into four parts, with the first introducing the basics of hydrogen bonding and important hydrogen bonding patterns in solution as well as in the solid state. The second part covers molecular recognition and supramolecular structures driven by hydrogen bonding. The third part introduces the formation of hollow and giant macrocycles directed by hydrogen bonding, while the last part summarizes hydrogen bonded supramolecular polymers. This book is designed to b

  15. Hydrogen in semiconductors

    CERN Document Server

    Pankove, Jacques I

    1991-01-01

    Hydrogen plays an important role in silicon technology, having a profound effect on a wide range of properties. Thus, the study of hydrogen in semiconductors has received much attention from an interdisciplinary assortment of researchers. This sixteen-chapter volume provides a comprehensive review of the field, including a discussion of hydrogenation methods, the use of hydrogen to passivate defects, the use of hydrogen to neutralize deep levels, shallow acceptors and shallow donors in silicon, vibrational spectroscopy, and hydrogen-induced defects in silicon. In addition to this detailed cove

  16. Hydrogen, this hallucinogen

    International Nuclear Information System (INIS)

    The author discusses the origin of hydrogen for energetic use (mainly by extraction from water), the possible uses of this cumbersome gas (in vehicles, in electricity storage), and outlines that hydrogen economy consumes a lot of other energies (nuclear, wind, sun, biomass, and so on) for a high cost, and that hydrogen is therefore not a solution for the future. Other elements are given in appendix: production methods and processes, figures of energy production, ways to use and to store hydrogen in vehicles, assessment of possibilities for a vehicle, techniques and figures for hydrogen packaging, transport and distribution, energy cost, energetic assessment of hydrogen production, problems associated with distribution (tank filling)

  17. A hydrogen ice cube

    OpenAIRE

    Schrauwers, A.

    2004-01-01

    Hydrogen is considered to be a highly promising energy carrier. Nonetheless, before hydrogen can become the fuel of choice for the future a number of slight problems will have to be overcome. For example, how can hydrogen be safely stored? Motor vehicles running on hydrogen may be clean in concept but where can we put the hydrogen? For many years now metal hydrides, which are compounds of metals and hydrogen, have been considered the perfect solution for this storage and safety problem but a ...

  18. Hydrogen-Assisted IC Engine Combustion as a Route to Hydrogen Implementation

    Energy Technology Data Exchange (ETDEWEB)

    Andre Boehman; Daniel Haworth

    2008-09-30

    composition and utilization through laboratory studies of spark-ignition engine operation on H{sub 2}-NG and numerical simulation of the impact of hydrogen blending on the physical and chemical processes within the engine; and (2) Examination of hydrogen-assisted combustion in advanced compression-ignition engine processes. To that end, numerical capabilities were applied to the study of hydrogen assisted combustion and experimental facilities were developed to achieve the project objectives.

  19. Boron-Based Hydrogen Storage: Ternary Borides and Beyond

    Energy Technology Data Exchange (ETDEWEB)

    Vajo, John J. [HRL Laboratories, LLC, Malibu, CA (United States)

    2016-04-28

    DOE continues to seek reversible solid-state hydrogen materials with hydrogen densities of ≥11 wt% and ≥80 g/L that can deliver hydrogen and be recharged at moderate temperatures (≤100 °C) and pressures (≤100 bar) enabling incorporation into hydrogen storage systems suitable for transportation applications. Boron-based hydrogen storage materials have the potential to meet the density requirements given boron’s low atomic weight, high chemical valance, and versatile chemistry. However, the rates of hydrogen exchange in boron-based compounds are thus far much too slow for practical applications. Although contributing to the high hydrogen densities, the high valance of boron also leads to slow rates of hydrogen exchange due to extensive boron-boron atom rearrangements during hydrogen cycling. This rearrangement often leads to multiple solid phases occurring over hydrogen release and recharge cycles. These phases must nucleate and react with each other across solid-solid phase boundaries leading to energy barriers that slow the rates of hydrogen exchange. This project sought to overcome the slow rates of hydrogen exchange in boron-based hydrogen storage materials by minimizing the number of solid phases and the boron atom rearrangement over a hydrogen release and recharge cycle. Two novel approaches were explored: 1) developing matched pairs of ternary borides and mixed-metal borohydrides that could exchange hydrogen with only one hydrogenated phase (the mixed-metal borohydride) and only one dehydrogenated phase (the ternary boride); and 2) developing boranes that could release hydrogen by being lithiated using lithium hydride with no boron-boron atom rearrangement.

  20. Calculation of LUEC using HEEP Software for Nuclear Hydrogen Production Plant

    International Nuclear Information System (INIS)

    To achieve the hydrogen economy, it is very important to produce a massive amount of hydrogen in a clean, safe and efficient way. Nuclear production of hydrogen would allow massive production of hydrogen at economic prices while avoiding environments pollution by reducing the release of carbon dioxide. A Very High Temperature Reactor (VHTR) is considered as an efficient reactor to couple with the thermo-chemical Sulfur Iodine (SI) cycle to achieve the hydrogen economy. HEEP(Hydrogen Economy Evaluation Program) is one of the software tools developed by IAEA to evaluate the economy of the nuclear hydrogen production system by estimating unit hydrogen production cost. In this paper, the LUHC (Levelized Unit Hydrogen Cost) is calculated by using HEEP for nuclear hydrogen production plant, which consists of 4 modules of 600 MWth VHTR coupled with SI process. The levelized unit hydrogen production cost(LUHC) was calculated by the HEEP software

  1. Calculation of LUEC using HEEP Software for Nuclear Hydrogen Production Plant

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jongho; Lee, Kiyoung; Kim, Minhwan [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-05-15

    To achieve the hydrogen economy, it is very important to produce a massive amount of hydrogen in a clean, safe and efficient way. Nuclear production of hydrogen would allow massive production of hydrogen at economic prices while avoiding environments pollution by reducing the release of carbon dioxide. A Very High Temperature Reactor (VHTR) is considered as an efficient reactor to couple with the thermo-chemical Sulfur Iodine (SI) cycle to achieve the hydrogen economy. HEEP(Hydrogen Economy Evaluation Program) is one of the software tools developed by IAEA to evaluate the economy of the nuclear hydrogen production system by estimating unit hydrogen production cost. In this paper, the LUHC (Levelized Unit Hydrogen Cost) is calculated by using HEEP for nuclear hydrogen production plant, which consists of 4 modules of 600 MWth VHTR coupled with SI process. The levelized unit hydrogen production cost(LUHC) was calculated by the HEEP software.

  2. Hydrogen production using high temperature nuclear reactors : A feasibility study

    OpenAIRE

    Sivertsson, Viktor

    2010-01-01

    The use of hydrogen is predicted to increase substantially in the future, both as chemical feedstock and also as energy carrier for transportation. The annual world production of hydrogen amounts to some 50 million tonnes and the majority is produced using fossil fuels like natural gas, coal and naphtha. High temperature nuclear reactors (HTRs) represent a novel way to produce hydrogen at large scale with high efficiency and less carbon footprint. The aim of this master thesis has been to eva...

  3. A Statistical Theory for Hydrogen Bonding Networks: One Component Case

    Institute of Scientific and Technical Information of China (English)

    WANG Hai-Jun; BA Xin-Wu; ZHAO Min; LI Ze-Sheng

    2000-01-01

    The theory of reversible gelation is shown to be applicable to the hydrogen bonding system by analyzing their similarities in statistical viewpoint. The size distribution of hydrogen bonding clusters, the gelation condition and the generalized scaling law can be obtained directly. These results show that such a system can undergo phase transition process. Furthermore, a relationship between Gibbs free energy of forming hydrogen bond and conversions of groups is given. As an example, the chemical shift of OH groups is considered.

  4. Fuel and Chemicals from Renewable Alcohols

    DEFF Research Database (Denmark)

    Hansen, Jeppe Rass

    2008-01-01

    The present work entitled Fuel and Chemicals from Renewable Alcohols covers the idea of developing routes for producing sustainable fuel and chemicals from biomass resources. Some renewable alcohols are already readily available from biomass in significant amounts and thus the potential...... be converted into hydrogen by steam reforming over nickel or ruthenium based catalysts. This process could be important in a future hydrogen society, where hydrogen can be utilized in high efficiency fuel cells. Hydrogen produced from biofeedstocks can also be used directly in the chemical industry, where...... it can compete with hydrogen production from natural gas. Similar substitution possibilities are emerging in the case of conversion of renewable alcohols to synthesis gas, which is used for instance in the manufacture of methanol and synthetic fuel. Here it is illustrated how glycerol can be converted...

  5. Performance characterization of a hydrogen catalytic heater.

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Terry Alan; Kanouff, Michael P.

    2010-04-01

    This report describes the performance of a high efficiency, compact heater that uses the catalytic oxidation of hydrogen to provide heat to the GM Hydrogen Storage Demonstration System. The heater was designed to transfer up to 30 kW of heat from the catalytic reaction to a circulating heat transfer fluid. The fluid then transfers the heat to one or more of the four hydrogen storage modules that make up the Demonstration System to drive off the chemically bound hydrogen. The heater consists of three main parts: (1) the reactor, (2) the gas heat recuperator, and (3) oil and gas flow distribution manifolds. The reactor and recuperator are integrated, compact, finned-plate heat exchangers to maximize heat transfer efficiency and minimize mass and volume. Detailed, three-dimensional, multi-physics computational models were used to design and optimize the system. At full power the heater was able to catalytically combust a 10% hydrogen/air mixture flowing at over 80 cubic feet per minute and transfer 30 kW of heat to a 30 gallon per minute flow of oil over a temperature range from 100 C to 220 C. The total efficiency of the catalytic heater, defined as the heat transferred to the oil divided by the inlet hydrogen chemical energy, was characterized and methods for improvement were investigated.

  6. Palladium Implanted Silicon Carbide for Hydrogen Sensing

    Science.gov (United States)

    Muntele, C. I.; Ila, D.; Zimmerman, R. L.; Muntele, L.; Poker, D. B.; Hensley, D. K.; Larkin, David (Technical Monitor)

    2001-01-01

    Silicon carbide is intended for use in fabrication of high-temperature, efficient hydrogen sensors. Traditionally, when a palladium coating is applied on the exposed surface of SiC, the chemical reaction between palladium and hydrogen produces a detectable change in the surface chemical potential. We have produced both a palladium coated SiC as well as a palladium, ion implanted SiC sensor. The palladium implantation was done at 500 C into the Si face of 6H, N-type SiC at various energies, and at various fluences. Then, we measured the hydrogen sensitivity response of each fabricated sensor by exposing them to hydrogen while monitoring the current flow across the p-n junction(s), with respect to time. The sensitivity of each sensor was measured at temperatures between 27 and 300 C. The response of the SiC sensors produced by Pd implantation has revealed a completely different behaviour than the SiC sensors produced by Pd deposition. In the Pd-deposited SiC sensors as well as in the ones reported in the literature, the current rises in the presence of hydrogen at room temperature as well as at elevated temperatures. In the case of Pd-implanted SiC sensors, the current decreases in the presence of hydrogen whenever the temperature is raised above 100 C. We will present the details and conclusions from the results obtained during this meeting.

  7. [Hydrogen peroxide in artificial photosynthesizing systems].

    Science.gov (United States)

    Lobanov, A V; Komissarov, G G

    2014-01-01

    From the point of view of the concepts of hydrogen peroxide as a source of photosynthetic oxygen (hydrogen) coordination and photochemical properties of chlorophyll and its aggregates towards hydrogen peroxide were considered. The binding energy of H2O and H2O2 with chlorophyll and chlorophyllide depending on their form (monomers, dimers and trimers) was estimated by quantum chemical calculations. It is shown that at an increase of the degree of the pigment aggregation binding energy of H2O2 was more than the energy of H2O. Analysis of experimental results of the photochemical decomposition of hydrogen peroxide using chlorophyll was carried out. Estimates of the thermodynamic parameters (deltaG degrees and deltaH degrees) of the formation of organic compounds from CO2 with water and hydrogen peroxide were compared. The interaction of CO2 with H2O2 requires much less energy consumption than with water for all considered cases. The formation of organic products (formaldehyde, alcohols, carboxylic and carbonylic compounds) and simultaneous production of O2 under the influence of visible light in the systems of inorganic carbon--hydrogen peroxide--chlorophyll (phthalocyanine) is detected by GC/MS method, FTIR spectroscopy, and chemical analysis. PMID:25702472

  8. Purification and analysis of hydrogen in SHMs

    International Nuclear Information System (INIS)

    Recently, the SHMs, as a functional material, has become an extremely important field of scientific research. Hydrogen produced from these materials have been mainly employed in the industry of energy, and was stored, transported, as a clean, un-contaminated artificial fuel (dual energy). SHMs being researched in the work now can be divided into four systems: such as Rare-Earth element system; Titanium system; Magnesium system; Vandium, Niobium, and Zirconium system. Several units of our country have been studied; hydrogen stored tanks that can produce super-high purity hydrogen with various SHMs, respectively. These tanks have been employed in electronic, metallurgical, chemical and other industries. Impurity content (such as O/sub 2/, Ar, CH/sub 4/, Co and CO/sub 2/ except water) of purified hydrogen can be less than 0.01 PPM. The purity of produced hydrogen can be comparable with that of purified by the palladium diffusive purifier. Besides, these equipments possess a lot of advantages, such as convenience, safety, reliability, long life time and low price. At present, chemical and electronic industries in high purity hydrogen always adopt low temperature adsorption, because of applying a large amount of liquid nitrogen, much energy consumed

  9. Chemical Emergencies

    Science.gov (United States)

    When a hazardous chemical has been released, it may harm people's health. Chemical releases can be unintentional, as in the case of an ... the case of a terrorist attack with a chemical weapon. Some hazardous chemicals have been developed by ...

  10. Dynamics of hydrogen in hydrogenated amorphous silicon

    Indian Academy of Sciences (India)

    Ranber Singh; S Prakash

    2003-07-01

    The problem of hydrogen diffusion in hydrogenated amorphous silicon (a-Si:H) is studied semiclassically. It is found that the local hydrogen concentration fluctuations-induced extra potential wells, if intense enough, lead to the localized electronic states in a-Si:H. These localized states are metastable. The trapping of electrons and holes in these states leads to the electrical degradation of the material. These states also act as recombination centers for photo-generated carriers (electrons and holes) which in turn may excite a hydrogen atom from a nearby Si–H bond and breaks the weak (strained) Si–Si bond thereby apparently enhancing the hydrogen diffusion and increasing the light-induced dangling bonds.

  11. Theoretical Study of Hydrogenated Tetrahedral Aluminum Clusters

    CERN Document Server

    Ichikawa, Kazuhide; Wagatsuma, Ayumu; Watanabe, Kouhei; Szarek, Pawel; Tachibana, Akitomo

    2011-01-01

    We report on the structures of aluminum hydrides derived from a tetrahedral aluminum Al4 cluster using ab initio quantum chemical calculation. Our calculation of binding energies of the aluminum hydrides reveals that stability of these hydrides increases as more hydrogen atoms are adsorbed, while stability of Al-H bonds decreases. We also analyze and discuss the chemical bonds of those clusters by using recently developed method based on the electronic stress tensor.

  12. Handbook of hydrogen energy

    CERN Document Server

    Sherif, SA; Stefanakos, EK; Steinfeld, Aldo

    2014-01-01

    ""This book provides an excellent overview of the hydrogen economy and a thorough and comprehensive presentation of hydrogen production and storage methods.""-Scott E. Grasman, Rochester Institute of Technology, New York, USA

  13. On hydrogen energy strategies

    International Nuclear Information System (INIS)

    This article focuses on hydrogen energy strategies. Possible problems regarding world stability, progress of hydrogen energy, possible strategies for hydrogen, and essential factors for hydrogen energy technologies are investigated and discussed in detail. Technical, environmental, sustainability and other perspectives are taken into consideration. The importance of hydrogen energy in reducing world problems and achieving a sustainable energy system is also investigated. It is seen that hydrogen energy can play an important role in reducing global problems and improving the sustainability of energy systems. Accordingly, hydrogen strategies based non-fossil energy sources should be developed to reduce world problems and unrest and to increase the level of sustainable development. It is expected that this article will contribute to the development of hydrogen energy strategies that is alternative to fossil-based strategies. (author)

  14. 21 CFR 520.62 - Aminopentamide hydrogen sulphate tablets.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Aminopentamide hydrogen sulphate tablets. 520.62 Section 520.62 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES... Aminopentamide hydrogen sulphate tablets. (a) Chemical name. 4-(Dimethylamino)-2,2-diphenylvaleramide...

  15. 40 CFR 721.4360 - Certain hydrogen containing chlorofluorocarbons.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Certain hydrogen containing chlorofluorocarbons. 721.4360 Section 721.4360 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.4360 Certain hydrogen containing chlorofluorocarbons. (a)...

  16. Solar Hydrogen Fuel Cell Projects at Brooklyn Tech

    Science.gov (United States)

    Fedotov, Alex; Farah, Shadia; Farley, Daithi; Ghani, Naureen; Kuo, Emmy; Aponte, Cecielo; Abrescia, Leo; Kwan, Laiyee; Khan, Ussamah; Khizner, Felix; Yam, Anthony; Sakeeb, Khan; Grey, Daniel; Anika, Zarin; Issa, Fouad; Boussayoud, Chayama; Abdeldayem, Mahmoud; Zhang, Alvin; Chen, Kelin; Chan, Kameron Chuen; Roytman, Viktor; Yee, Michael

    2010-01-01

    This article describes the projects on solar hydrogen powered vehicles using water as fuel conducted by teams at Brooklyn Technical High School. Their investigations into the pure and applied chemical thermodynamics of hydrogen fuel cells and bio-inspired devices have been consolidated in a new and emerging sub-discipline that they define as solar…

  17. Investigation of the explosion hazards of hydrogen sulphide

    International Nuclear Information System (INIS)

    The results of Phase I of an investigation directed towards quantifying the explosion hazards of hydrogen sulphide in air are described. The first phase is focussed on detonation in free hydrogen sulphide/air clouds. Detonation properties, including velocity and pressure, have been calculated and compared with experimental results. The observed detonation structure together with critical tube tests tests are used to assess the detonability of hydrogen sulphide/air mixtures relative to hydrogen and common hydrocarbon gases. Detailed chemical kinetic modelling of hydrogen sulphide combustion in air has been performed to correlate the detonation cell size data and to determine the influence of water vapour on the detonability of hydrogen sulphide in air. Calculations of the blast wave properties for detonation of a hydrogen sulphide/air cloud provide the data required to assess the blast effects of such explosions

  18. Doping in the Valley of Hydrogen Solubility: A Route to Designing Hydrogen-Resistant Zirconium Alloys

    Science.gov (United States)

    Youssef, Mostafa; Yang, Ming; Yildiz, Bilge

    2016-01-01

    Hydrogen pickup and embrittlement pose a challenging safety limit for structural alloys used in a wide range of infrastructure applications, including zirconium alloys in nuclear reactors. Previous experimental observations guide the empirical design of hydrogen-resistant zirconium alloys, but the underlying mechanisms remain undecipherable. Here, we assess two critical prongs of hydrogen pickup through the ZrO2 passive film that serves as a surface barrier of zirconium alloys; the solubility of hydrogen in it—a detrimental process—and the ease of H2 gas evolution from its surface—a desirable process. By combining statistical thermodynamics and density-functional-theory calculations, we show that hydrogen solubility in ZrO2 exhibits a valley shape as a function of the chemical potential of electrons, μe . Here, μe , which is tunable by doping, serves as a physical descriptor of hydrogen resistance based on the electronic structure of ZrO2 . For designing zirconium alloys resistant against hydrogen pickup, we target either a dopant that thermodynamically minimizes the solubility of hydrogen in ZrO2 at the bottom of this valley (such as Cr) or a dopant that maximizes μe and kinetically accelerates proton reduction and H2 evolution at the surface of ZrO2 (such as Nb, Ta, Mo, W, or P). Maximizing μe also promotes the predomination of a less-mobile form of hydrogen defect, which can reduce the flux of hydrogen uptake. The analysis presented here for the case of ZrO2 passive film on Zr alloys serves as a broadly applicable and physically informed framework to uncover doping strategies to mitigate hydrogen embrittlement also in other alloys, such as austenitic steels or nickel alloys, which absorb hydrogen through their surface oxide films.

  19. Hydrogen Sulfide Micro-Sensor for Biomass Fouling Detection Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Hydrogen Sulfide (H2S)is the leading chemical agent causing human fatalities following inhalation exposures. The overall aim of this project is to develop and...

  20. Chemical composition and structure of particles synthesized on the surface of HHPC in nuclear reactions induced by bremstrahlung γ quanta with threshold energy of 10 MeV in molecular hydrogen at a pressure of 0.5 kbar

    Science.gov (United States)

    Didyk, A. Yu.; Wiśniewski, R.

    2015-12-01

    A high-pressure chamber filled with molecular hydrogen (HHPC) at a pressure of 0.5 kbar with a Pd rod inside has been irradiated for 14 h with γ quanta with an energy of 9.7 kbar produced by an electron beam current of 20-21 μA. Postirradiation studies of the changes in the structure of the synthesized particle and other objects on the surface of a brass hub in the composition of HHPC revealed the presence of light elements from carbon to calcium. Multiple small particles of lead have also been found and studied. The detected synthesized particle has complex shape and composition. Also, thin-walled microtubes were detected on the inner surfaces inside HHPC. Based on fission reactions of intermediate mass nuclei (descending reactions), as well as the reactions of synthesis from hydrogen and heavier nuclei (ascending reactions), an attempt to explain the anomalies that were observed is made.

  1. Nuclear electrolytic hydrogen

    International Nuclear Information System (INIS)

    An extensive study of hydrogen supply has recently been carried out by Ontario Hydro which indicates that electrolytic hydrogen produced from nuclear electricity could offer the lowest cost option for any future large scale hydrogen supply in the Province of Ontario, Canada. This paper provides a synopsis of the Ontario Hydro study, a brief overview of the economic factors supporting the study conclusion and discussion of a number of issues concerning the supply of electrolytic hydrogen by electric power utilities

  2. Hydrogen Technologies Safety Guide

    Energy Technology Data Exchange (ETDEWEB)

    Rivkin, C. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Burgess, R. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Buttner, W. [National Renewable Energy Lab. (NREL), Golden, CO (United States)

    2015-01-01

    The purpose of this guide is to provide basic background information on hydrogen technologies. It is intended to provide project developers, code officials, and other interested parties the background information to be able to put hydrogen safety in context. For example, code officials reviewing permit applications for hydrogen projects will get an understanding of the industrial history of hydrogen, basic safety concerns, and safety requirements.

  3. Hydrogen Embrittlement of Hydro-Cracker Pipe

    International Nuclear Information System (INIS)

    Low carbon steel elbows of the hydro-cracker pipe in an oil refinery plant were failed after six months operation. The elbows were manufactured according to ASTM A234 WPB, which specifies the processing requirements for the parts used in sour gas environment. The chemical compositions, mechanical properties, microstructures and crack morphologies were evaluated and compared to ASTM specification. It was found that ingress of hydrogen with the aid of hydrogen sulfide to the deformed area drove the parts to the failure. The deformed structures in failed elbows, which resulted in high hardness and low ductility, enhanced sulfide stress cracking(SSC) in sour gas service. The effects of normalizing and cold working on the sulfide stress cracking were simulated by electrolytic hydrogen charging. It was found that normalized steel was not susceptible to SSC after the hydrogen charging. The preventive measures against SSC were discussed

  4. Catalytic hydrogenation of carbon monoxide

    Energy Technology Data Exchange (ETDEWEB)

    Wayland, B.B.

    1992-12-01

    This project is focused on developing strategies to accomplish the reduction and hydrogenation of carbon monoxide to produce organic oxygenates at mild conditions. Our approaches to this issue are based on the recognition that rhodium macrocycles have unusually favorable thermodynamic values for producing a series of intermediate implicated in the catalytic hydrogenation of CO. Observations of metalloformyl complexes produced by reactions of H{sub 2} and CO, and reductive coupling of CO to form metallo {alpha}-diketone species have suggested a multiplicity of routes to organic oxygenates that utilize these species as intermediates. Thermodynamic and kinetic-mechanistic studies are used in constructing energy profiles for a variety of potential pathways, and these schemes are used in guiding the design of new metallospecies to improve the thermodynamic and kinetic factors for individual steps in the overall process. Variation of the electronic and steric effects associated with the ligand arrays along with the influences of the reaction medium provide the chemical tools for tuning these factors. Emerging knowledge of the factors that contribute to M-H, M-C and M-O bond enthalpies is directing the search for ligand arrays that will expand the range of metal species that have favorable thermodynamic parameters to produce the primary intermediates for CO hydrogenation. Studies of rhodium complexes are being extended to non-macrocyclic ligand complexes that emulate the favorable thermodynamic features associated with rhodium macrocycles, but that also manifest improved reaction kinetics. Multifunctional catalyst systems designed to couple the ability of rhodium complexes to produce formyl and diketone intermediates with a second catalyst that hydrogenates these imtermediates are promising approaches to accomplish CO hydrogenation at mild conditions.

  5. Metallic Hydrogen: A Game Changing Rocket Propellant

    Science.gov (United States)

    Silvera, Isaac F.

    2016-01-01

    The objective of this research is to produce metallic hydrogen in the laboratory using an innovative approach, and to study its metastability properties. Current theoretical and experimental considerations expect that extremely high pressures of order 4-6 megabar are required to transform molecular hydrogen to the metallic phase. When metallic hydrogen is produced in the laboratory it will be extremely important to determine if it is metastable at modest temperatures, i.e. remains metallic when the pressure is released. Then it could be used as the most powerful chemical rocket fuel that exists and revolutionize rocketry, allowing single-stage rockets to enter orbit and chemically fueled rockets to explore our solar system.

  6. Illustrating Chemical Concepts through Food Systems: Introductory Chemistry Experiments.

    Science.gov (United States)

    Chambers, E., IV; Setser, C. S.

    1980-01-01

    Demonstrations involving foods that illustrate chemical concepts are described, including vaporization of liquids and Graham's law of diffusion, chemical reaction rates, adsorption, properties of solutions, colloidal dispersions, suspensions, and hydrogen ion concentration. (CS)

  7. Biological hydrogen photoproduction

    Energy Technology Data Exchange (ETDEWEB)

    Nemoto, Y. [Univ. of Miami, FL (United States)

    1995-09-01

    Following are the major accomplishments of the 6th year`s study of biological hydrogen photoproduction which were supported by DOE/NREL. (1) We have been characterizing a biological hydrogen production system using synchronously growing aerobically nitrogen-fixing unicellular cyanobacterium, Synechococcus sp. Miami BG 043511. So far it was necessary to irradiate the cells to produce hydrogen. Under darkness they did not produce hydrogen. However, we found that, if the cells are incubated with oxygen, they produce hydrogen under the dark. Under 80% argon + 20% oxygen condition, the hydrogen production activity under the dark was about one third of that under the light + argon condition. (2) Also it was necessary so far to incubate the cells under argon atmosphere to produce hydrogen in this system. Argon treatment is very expensive and should be avoided in an actual hydrogen production system. We found that, if the cells are incubated at a high cell density and in a container with minimum headspace, it is not necessary to use argon for the hydrogen production. (3) Calcium ion was found to play an important role in the mechanisms of protection of nitrogenase from external oxygen. This will be a clue to understand the reason why the hydrogen production is so resistant to oxygen in this strain. (4) In this strain, sulfide can be used as electron donor for the hydrogen production. This result shows that waste water can be used for the hydrogen production system using this strain.

  8. Magnesium for Hydrogen Storage

    DEFF Research Database (Denmark)

    Vigeholm, B.; Kjøller, John; Larsen, Bent

    1980-01-01

    The reaction of hydrogen with commercially pure magnesium powder (above 99.7%) was investigated in the temperature range 250–400 °C. Hydrogen is readily sorbed above the dissociation pressure. During the initial exposure the magnesium powder sorbs hydrogen slowly below 400 °C but during the second...

  9. HGMS: Glasses and Nanocomposites for Hydrogen Storage.

    Energy Technology Data Exchange (ETDEWEB)

    Lipinska, Kris [PI; Hemmers, Oliver

    2013-02-17

    The primary goal of this project is to fabricate and investigate different glass systems and glass-derived nanocrystalline composite materials. These glass-based, two-phased materials will contain nanocrystals that can attract hydrogen and be of potential interest as hydrogen storage media. The glass materials with intrinsic void spaces that are able to precipitate functional nanocrystals capable to attract hydrogen are of particular interest. Proposed previously, but never practically implemented, one of promising concepts for storing hydrogen are micro-containers built of glass and shaped into hollow microspheres. The project expanded this concept to the exploration of glass-derived nanocrystalline composites as potential hydrogen storage media. It is known that the most desirable materials for hydrogen storage do not interact chemically with hydrogen and possess a high surface area to host substantial amounts of hydrogen. Glasses are built of disordered networks with ample void spaces that make them permeable to hydrogen even at room temperature. Glass-derived nanocrystalline composites (two-phased materials), combination of glasses (networks with ample voids) and functional nanocrystals (capable to attract hydrogen), appear to be promising candidates for hydrogen storage media. Key advantages of glass materials include simplicity of preparation, flexibility of composition, chemical durability, non-toxicity and mechanical strength, as well as low production costs and environmental friendliness. This project encompasses a fundamental research into physics and chemistry of glasses and nanocrystalline composite materials, derived from glass. Studies are aimed to answer questions essential for considering glass-based materials and composites as potential hydrogen storage media. Of particular interest are two-phased materials that combine glasses with intrinsic voids spaces for physisorption of hydrogen and nanocrystals capable of chemisorption. This project does not

  10. Numerical Study on the Acetylene Concentration in the Hydrogen-Carbon System in a Hydrogen Plasma Torch

    Institute of Scientific and Technical Information of China (English)

    CHEN Longwei; SHEN Jie; SHU Xingsheng; FANG Shidong; ZHANG Lipeng; MENG Yuedong

    2009-01-01

    Effects of the hydrogen/carbon mole ratio and pyrolysis gas pressure on the acetylene concentration in the hydrogen-carbon system in a plasma torch were numerically calculated by using the chemical thermodynamic equilibrium method of Gibbs free energy. The calculated results indicate that the hydrogen concentration and the pyrolysis gas pressure play crucial roles in acetylene formation. Appropriately abundant hydrogen, with a mole ratio of hydrogen to carbon about 1 or 2, and a relatively high pyrolysis gas pressure can enhance the acetylene concentration. In the experiment, a compromised project consisting of an appropriate hydrogen flow rate and a feasible high pyrolysis gas pressure needs to be carried out to increase the acetylene concentration from coal pyrolysis in the hydrogen plasma torch.

  11. Novel Hydrogen Bioreactor and Detection Apparatus.

    Science.gov (United States)

    Rollin, Joseph A; Ye, Xinhao; Del Campo, Julia Martin; Adams, Michael W W; Zhang, Y-H Percival

    2016-01-01

    In vitro hydrogen generation represents a clear opportunity for novel bioreactor and system design. Hydrogen, already a globally important commodity chemical, has the potential to become the dominant transportation fuel of the future. Technologies such as in vitro synthetic pathway biotransformation (SyPaB)-the use of more than 10 purified enzymes to catalyze unnatural catabolic pathways-enable the storage of hydrogen in the form of carbohydrates. Biohydrogen production from local carbohydrate resources offers a solution to the most pressing challenges to vehicular and bioenergy uses: small-size distributed production, minimization of CO2 emissions, and potential low cost, driven by high yield and volumetric productivity. In this study, we introduce a novel bioreactor that provides the oxygen-free gas phase necessary for enzymatic hydrogen generation while regulating temperature and reactor volume. A variety of techniques are currently used for laboratory detection of biohydrogen, but the most information is provided by a continuous low-cost hydrogen sensor. Most such systems currently use electrolysis for calibration; here an alternative method, flow calibration, is introduced. This system is further demonstrated here with the conversion of glucose to hydrogen at a high rate, and the production of hydrogen from glucose 6-phosphate at a greatly increased reaction rate, 157 mmol/L/h at 60 °C. PMID:25022362

  12. Novel Hydrogen Bioreactor and Detection Apparatus.

    Science.gov (United States)

    Rollin, Joseph A; Ye, Xinhao; Del Campo, Julia Martin; Adams, Michael W W; Zhang, Y-H Percival

    2016-01-01

    In vitro hydrogen generation represents a clear opportunity for novel bioreactor and system design. Hydrogen, already a globally important commodity chemical, has the potential to become the dominant transportation fuel of the future. Technologies such as in vitro synthetic pathway biotransformation (SyPaB)-the use of more than 10 purified enzymes to catalyze unnatural catabolic pathways-enable the storage of hydrogen in the form of carbohydrates. Biohydrogen production from local carbohydrate resources offers a solution to the most pressing challenges to vehicular and bioenergy uses: small-size distributed production, minimization of CO2 emissions, and potential low cost, driven by high yield and volumetric productivity. In this study, we introduce a novel bioreactor that provides the oxygen-free gas phase necessary for enzymatic hydrogen generation while regulating temperature and reactor volume. A variety of techniques are currently used for laboratory detection of biohydrogen, but the most information is provided by a continuous low-cost hydrogen sensor. Most such systems currently use electrolysis for calibration; here an alternative method, flow calibration, is introduced. This system is further demonstrated here with the conversion of glucose to hydrogen at a high rate, and the production of hydrogen from glucose 6-phosphate at a greatly increased reaction rate, 157 mmol/L/h at 60 °C.

  13. Biological hydrogen formation by thermophilic bacteria

    NARCIS (Netherlands)

    Bielen, A.A.M.

    2014-01-01

      Hydrogen gas (H2) is an important chemical commodity. It is used in many industrial processes and is applicable as a fuel. However, present production processes are predominantly based on non-renewable resources. In a biological H2 (bioH2) production process,

  14. Thermophysical properties of warm dense hydrogen

    CERN Document Server

    Holst, Bastian; Desjarlais, Michael P

    2007-01-01

    We study the thermophysical properties of warm dense hydrogen using quantum molecular dynamics simulations. New results are presented for the pair distribution functions, the equation of state, the Hugoniot curve, and the reflectivity. We compare with available experimental data and predictions of the chemical picture. Especially, we discuss the nonmetal-to-metal transition which occurs at about 40 GPa in the dense fluid.

  15. Electricity-mediated biological hydrogen production

    NARCIS (Netherlands)

    Geelhoed, J.S.; Hamelers, H.V.M.; Stams, A.J.M.

    2010-01-01

    Anaerobic bacteria have the ability to produce electricity from the oxidation of organic substrates. They also may use electricity to support chemical reactions that are energetically unfavorable. In the fermentation of sugars, hydrogen can be formed as one of the main products. However, a yield of

  16. Overview of interstate hydrogen pipeline systems.

    Energy Technology Data Exchange (ETDEWEB)

    Gillette, J .L.; Kolpa, R. L

    2008-02-01

    The use of hydrogen in the energy sector of the United States is projected to increase significantly in the future. Current uses are predominantly in the petroleum refining sector, with hydrogen also being used in the manufacture of chemicals and other specialized products. Growth in hydrogen consumption is likely to appear in the refining sector, where greater quantities of hydrogen will be required as the quality of the raw crude decreases, and in the mining and processing of tar sands and other energy resources that are not currently used at a significant level. Furthermore, the use of hydrogen as a transportation fuel has been proposed both by automobile manufacturers and the federal government. Assuming that the use of hydrogen will significantly increase in the future, there would be a corresponding need to transport this material. A variety of production technologies are available for making hydrogen, and there are equally varied raw materials. Potential raw materials include natural gas, coal, nuclear fuel, and renewables such as solar, wind, or wave energy. As these raw materials are not uniformly distributed throughout the United States, it would be necessary to transport either the raw materials or the hydrogen long distances to the appropriate markets. While hydrogen may be transported in a number of possible forms, pipelines currently appear to be the most economical means of moving it in large quantities over great distances. One means of controlling hydrogen pipeline costs is to use common rights-of-way (ROWs) whenever feasible. For that reason, information on hydrogen pipelines is the focus of this document. Many of the features of hydrogen pipelines are similar to those of natural gas pipelines. Furthermore, as hydrogen pipeline networks expand, many of the same construction and operating features of natural gas networks would be replicated. As a result, the description of hydrogen pipelines will be very similar to that of natural gas pipelines

  17. Hydrogen separation process

    Science.gov (United States)

    Mundschau, Michael; Xie, Xiaobing; Evenson, IV, Carl; Grimmer, Paul; Wright, Harold

    2011-05-24

    A method for separating a hydrogen-rich product stream from a feed stream comprising hydrogen and at least one carbon-containing gas, comprising feeding the feed stream, at an inlet pressure greater than atmospheric pressure and a temperature greater than 200.degree. C., to a hydrogen separation membrane system comprising a membrane that is selectively permeable to hydrogen, and producing a hydrogen-rich permeate product stream on the permeate side of the membrane and a carbon dioxide-rich product raffinate stream on the raffinate side of the membrane. A method for separating a hydrogen-rich product stream from a feed stream comprising hydrogen and at least one carbon-containing gas, comprising feeding the feed stream, at an inlet pressure greater than atmospheric pressure and a temperature greater than 200.degree. C., to an integrated water gas shift/hydrogen separation membrane system wherein the hydrogen separation membrane system comprises a membrane that is selectively permeable to hydrogen, and producing a hydrogen-rich permeate product stream on the permeate side of the membrane and a carbon dioxide-rich product raffinate stream on the raffinate side of the membrane. A method for pretreating a membrane, comprising: heating the membrane to a desired operating temperature and desired feed pressure in a flow of inert gas for a sufficient time to cause the membrane to mechanically deform; decreasing the feed pressure to approximately ambient pressure; and optionally, flowing an oxidizing agent across the membrane before, during, or after deformation of the membrane. A method of supporting a hydrogen separation membrane system comprising selecting a hydrogen separation membrane system comprising one or more catalyst outer layers deposited on a hydrogen transport membrane layer and sealing the hydrogen separation membrane system to a porous support.

  18. Hydrogen Bonds Involving Metal Centers

    OpenAIRE

    Pavlović, G.; Raos, N.

    2006-01-01

    Hydrogen bonds involving metal center as a hydrogen donor or hydrogen acceptor are only a specific type of metal-hydrogen interactions; it is therefore not easy to differentiate hydrogen bond from other metal-hydrogen interactions, especially agostic ones. The first part of the review is therefore devoted to the results of structural chemistry and molecular spectroscopy (NMR, IR), as a tool for differentiating hydrogen bondings from other hydrogen interactions. The classical examples of Pt···...

  19. Final Report: Metal Perhydrides for Hydrogen Storage

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, J-Y.; Shi, S.; Hackney, S.; Swenson, D.; Hu, Y.

    2011-07-26

    Hydrogen is a promising energy source for the future economy due to its environmental friendliness. One of the important obstacles for the utilization of hydrogen as a fuel source for applications such as fuel cells is the storage of hydrogen. In the infrastructure of the expected hydrogen economy, hydrogen storage is one of the key enabling technologies. Although hydrogen possesses the highest gravimetric energy content (142 KJ/g) of all fuels, its volumetric energy density (8 MJ/L) is very low. It is desired to increase the volumetric energy density of hydrogen in a system to satisfy various applications. Research on hydrogen storage has been pursed for many years. Various storage technologies, including liquefaction, compression, metal hydride, chemical hydride, and adsorption, have been examined. Liquefaction and high pressure compression are not desired due to concerns related to complicated devices, high energy cost and safety. Metal hydrides and chemical hydrides have high gravimetric and volumetric energy densities but encounter issues because high temperature is required for the release of hydrogen, due to the strong bonding of hydrogen in the compounds. Reversibility of hydrogen loading and unloading is another concern. Adsorption of hydrogen on high surface area sorbents such as activated carbon and organic metal frameworks does not have the reversibility problem. But on the other hand, the weak force (primarily the van der Waals force) between hydrogen and the sorbent yields a very small amount of adsorption capacity at ambient temperature. Significant storage capacity can only be achieved at low temperatures such as 77K. The use of liquid nitrogen in a hydrogen storage system is not practical. Perhydrides are proposed as novel hydrogen storage materials that may overcome barriers slowing advances to a hydrogen fuel economy. In conventional hydrides, e.g. metal hydrides, the number of hydrogen atoms equals the total valence of the metal ions. One Li

  20. Hydrogen energy assessment

    Energy Technology Data Exchange (ETDEWEB)

    Salzano, F J; Braun, C [eds.

    1977-09-01

    The purpose of this assessment is to define the near term and long term prospects for the use of hydrogen as an energy delivery medium. Possible applications of hydrogen are defined along with the associated technologies required for implementation. A major focus in the near term is on industrial uses of hydrogen for special applications. The major source of hydrogen in the near term is expected to be from coal, with hydrogen from electric sources supplying a smaller fraction. A number of potential applications for hydrogen in the long term are identified and the level of demand estimated. The results of a cost benefit study for R and D work on coal gasification to hydrogen and electrolytic production of hydrogen are presented in order to aid in defining approximate levels of R and D funding. A considerable amount of data is presented on the cost of producing hydrogen from various energy resources. A key conclusion of the study is that in time hydrogen is likely to play a role in the energy system; however, hydrogen is not yet competitive for most applications when compared to the cost of energy from petroleum and natural gas.

  1. Photobiological hydrogen production.

    Science.gov (United States)

    Asada, Y; Miyake, J

    1999-01-01

    The principles and recent progress in the research and development of photobiological hydrogen production are reviewed. Cyanobacteria produce hydrogen gas using nitrogenase and/or hydrogenase. Hydrogen production mediated by native hydrogenases in cyanobacteria occurs under in the dark under anaerobic conditions by degradation of intracellular glycogen. In vitro and in vivo coupling of the cyanobacterial photosynthetic system with a clostridial hydrogenase via cyanobacterial ferredoxin was demonstrated in the presence of light. Genetic transformation of Synechococcus PCC7942 with the hydrogenase gene from Clostridium pasteurianum was successful; the active enzyme was expressed in PCC7942. The strong hydrogen producers among photosynthetic bacteria were isolated and characterized. Coculture of Rhodobacter and Clostriudium was applied for hydrogen production from glucose. A mutant strain of Rhodobacter sphaeroides RV whose light-harvesting proteins were altered was obtained by UV irradiation. Hydrogen productivity by the mutant was improved when irradiated with monochromatic light of some wavelengths. The development of photobioreactors for hydrogen production is also reviewed.

  2. Hydrogen energy for beginners

    CERN Document Server

    2013-01-01

    This book highlights the outstanding role of hydrogen in energy processes, where it is the most functional element due to its unique peculiarities that are highlighted and emphasized in the book. The first half of the book covers the great natural hydrogen processes in biology, chemistry, and physics, showing that hydrogen is a trend that can unite all natural sciences. The second half of the book is devoted to the technological hydrogen processes that are under research and development with the aim to create the infrastructure for hydrogen energetics. The book describes the main features of hydrogen that make it inalienable player in processes such as fusion, photosynthesis, and metabolism. It also covers the methods of hydrogen production and storage, highlighting at the same time the exclusive importance of nanotechnologies in those processes.

  3. Theoretical description of hydrogen bonding in oxalic acid dimer and trimer based on the combined extended-transition-state energy decomposition analysis and natural orbitals for chemical valence (ETS-NOCV)

    Science.gov (United States)

    Mitoraj, Mariusz P.; Kurczab, Rafał; Boczar, Marek

    2010-01-01

    In the present study we have analyzed hydrogen bonding in dimer and trimer of oxalic acid, based on a recently proposed charge and energy decomposition scheme (ETS-NOCV). In the case of a dimer, two conformations, α and β, were considered. The deformation density contributions originating from NOCV’s revealed that the formation of hydrogen bonding is associated with the electronic charge deformation in both the σ—(Δρσ) and π-networks (Δρπ). It was demonstrated that σ-donation is realized by electron transfer from the lone pair of oxygen on one monomer into the empty \\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ \\rho_{H - O}^* $$\\end{document} orbital of the second oxalic acid fragment. In addition, a covalent contribution is observed by the density transfer from hydrogen of H-O group in one oxalic acid monomer to the oxygen atom of the second fragment. The resonance assisted component (Δρπ), is based on the transfer of electron density from the π—orbital localized on the oxygen of OH on one oxalic acid monomer to the oxygen atom of the other fragment. ETS-NOCV allowed to conclude that the σ(O---HO) component is roughly eight times as important as π (RAHB) contribution in terms of energetic estimation. The electrostatic factor (ΔEelstat) is equally as important as orbital interaction term (ΔEorb). Finally, comparing β-dimer of oxalic acid with trimer we found practically no difference concerning each of the O---HO bonds, neither qualitative nor quantitative. Figure The contours of deformation density σ- and π-contributions describing the hydrogen bonding between the monomers in the oxalic acid dimer, together with the corresponding ETS-NOCV-based orbital-interaction energies (in kcal/mol). PMID:20505966

  4. 21 CFR 522.1222b - Ketamine hydrochloride with promazine hydrochloride and aminopentamide hydrogen sulfate injection.

    Science.gov (United States)

    2010-04-01

    ... hydrochloride and aminopentamide hydrogen sulfate injection. 522.1222b Section 522.1222b Food and Drugs FOOD AND... hydrochloride with promazine hydrochloride and aminopentamide hydrogen sulfate injection. (a) Chemical name... hydrochloride, 10- phenothiazine monohydrochloride, and aminopentamide hydrogen sulfate. (b) Specifications....

  5. Application of Hydrogen for the Reduction of Bauxite Mineral

    Science.gov (United States)

    Parhi, B. R.; Sahoo, S. K.; Bhoi, B.; Satapathy, B. K.; Paramguru, R. K.

    2016-02-01

    Reduction of oxides present in bauxite through hydrogen was investigated in the present study. The bauxite samples were subjected to reduction through molecular hydrogen and hydrogen plasma at 650oC and 800oC with different flow rates of hydrogen for different time periods respectively. The samples, after the reduction processes, were characterized by X-ray diffraction technique and chemical analysis. It was observed that the oxides of iron present in bauxite were only undergone through reduction while other oxides remain unreduced. An attempt was then made to separate pure Al2O3 present in bauxite samples through acid leaching process.

  6. Study on stability of hydrogenated amorphous silicon films

    Institute of Scientific and Technical Information of China (English)

    Zhu Xiu-Hong; Chen Guang-Hua; Zhang Wen-Li; Ding Yi; Ma Zhan-Jie; Hu Yue-Hui; He Bin; Rong Yan-Dong

    2005-01-01

    Hydrogenated amorphous silicon (a-Si:H) films with high and same order of magnitude photosensitivity (~105) but different stability were prepared by using microwave electron cyclotron resonance chemical vapour deposition system under the different deposition conditions. It was proposed that there was no direct correlation between the photosensitivity and the hydrogen content (CH) as well as H-Si bonding configurations, but for the stability, they were the critical factors. The experimental results indicated that higher substrate temperature, hydrogen dilution ratio and lower deposition rate played an important role in improving the microstructure of a-Si:H films. We used hydrogen elimination model to explain our experimental results.

  7. Hydrogen Filling Station

    Energy Technology Data Exchange (ETDEWEB)

    Boehm, Robert F; Sabacky, Bruce; Anderson II, Everett B; Haberman, David; Al-Hassin, Mowafak; He, Xiaoming; Morriseau, Brian

    2010-02-24

    Hydrogen is an environmentally attractive transportation fuel that has the potential to displace fossil fuels. The Freedom CAR and Freedom FUEL initiatives emphasize the importance of hydrogen as a future transportation fuel. Presently, Las Vegas has one hydrogen fueling station powered by natural gas. However, the use of traditional sources of energy to produce hydrogen does not maximize the benefit. The hydrogen fueling station developed under this grant used electrolysis units and solar energy to produce hydrogen fuel. Water and electricity are furnished to the unit and the output is hydrogen and oxygen. Three vehicles were converted to utilize the hydrogen produced at the station. The vehicles were all equipped with different types of technologies. The vehicles were used in the day-to-day operation of the Las Vegas Valley Water District and monitoring was performed on efficiency, reliability and maintenance requirements. The research and demonstration utilized for the reconfiguration of these vehicles could lead to new technologies in vehicle development that could make hydrogen-fueled vehicles more cost effective, economical, efficient and more widely used. In order to advance the development of a hydrogen future in Southern Nevada, project partners recognized a need to bring various entities involved in hydrogen development and deployment together as a means of sharing knowledge and eliminating duplication of efforts. A road-mapping session was held in Las Vegas in June 2006. The Nevada State Energy Office, representatives from DOE, DOE contractors and LANL, NETL, NREL were present. Leadership from the National hydrogen Association Board of Directors also attended. As a result of this session, a roadmap for hydrogen development was created. This roadmap has the ability to become a tool for use by other road-mapping efforts in the hydrogen community. It could also become a standard template for other states or even countries to approach planning for a hydrogen

  8. Hydrogen Filling Station

    Energy Technology Data Exchange (ETDEWEB)

    Boehm, Robert F; Sabacky, Bruce; Anderson II, Everett B; Haberman, David; Al-Hassin, Mowafak; He, Xiaoming; Morriseau, Brian

    2010-02-24

    Hydrogen is an environmentally attractive transportation fuel that has the potential to displace fossil fuels. The Freedom CAR and Freedom FUEL initiatives emphasize the importance of hydrogen as a future transportation fuel. Presently, Las Vegas has one hydrogen fueling station powered by natural gas. However, the use of traditional sources of energy to produce hydrogen does not maximize the benefit. The hydrogen fueling station developed under this grant used electrolysis units and solar energy to produce hydrogen fuel. Water and electricity are furnished to the unit and the output is hydrogen and oxygen. Three vehicles were converted to utilize the hydrogen produced at the station. The vehicles were all equipped with different types of technologies. The vehicles were used in the day-to-day operation of the Las Vegas Valley Water District and monitoring was performed on efficiency, reliability and maintenance requirements. The research and demonstration utilized for the reconfiguration of these vehicles could lead to new technologies in vehicle development that could make hydrogen-fueled vehicles more cost effective, economical, efficient and more widely used. In order to advance the development of a hydrogen future in Southern Nevada, project partners recognized a need to bring various entities involved in hydrogen development and deployment together as a means of sharing knowledge and eliminating duplication of efforts. A road-mapping session was held in Las Vegas in June 2006. The Nevada State Energy Office, representatives from DOE, DOE contractors and LANL, NETL, NREL were present. Leadership from the National hydrogen Association Board of Directors also attended. As a result of this session, a roadmap for hydrogen development was created. This roadmap has the ability to become a tool for use by other road-mapping efforts in the hydrogen community. It could also become a standard template for other states or even countries to approach planning for a hydrogen

  9. Hydrogen Fuel Cells and Storage Technology: Fundamental Research for Optimization of Hydrogen Storage and Utilization

    Energy Technology Data Exchange (ETDEWEB)

    Perret, Bob; Heske, Clemens; Nadavalath, Balakrishnan; Cornelius, Andrew; Hatchett, David; Bae, Chusung; Pang, Tao; Kim, Eunja; Hemmers, Oliver

    2011-03-28

    Design and development of improved low-cost hydrogen fuel cell catalytic materials and high-capacity hydrogenn storage media are paramount to enabling the hydrogen economy. Presently, effective and durable catalysts are mostly precious metals in pure or alloyed form and their high cost inhibits fuel cell applications. Similarly, materials that meet on-board hydrogen storage targets within total mass and volumetric constraints are yet to be found. Both hydrogen storage performance and cost-effective fuel cell designs are intimately linked to the electronic structure, morphology and cost of the chosen materials. The FCAST Project combined theoretical and experimental studies of electronic structure, chemical bonding, and hydrogen adsorption/desorption characteristics of a number of different nanomaterials and metal clusters to develop better fundamental understanding of hydrogen storage in solid state matrices. Additional experimental studies quantified the hydrogen storage properties of synthesized polyaniline(PANI)/Pd composites. Such conducting polymers are especially interesting because of their high intrinsic electron density and the ability to dope the materials with protons, anions, and metal species. Earlier work produced contradictory results: one study reported 7% to 8% hydrogen uptake while a second study reported zero hydrogen uptake. Cost and durability of fuel cell systems are crucial factors in their affordability. Limits on operating temperature, loss of catalytic reactivity and degradation of proton exchange membranes are factors that affect system durability and contribute to operational costs. More cost effective fuel cell components were sought through studies of the physical and chemical nature of catalyst performance, characterization of oxidation and reduction processes on system surfaces. Additional development effort resulted in a new hydrocarbon-based high-performance sulfonated proton exchange membrane (PEM) that can be manufactured at low

  10. Canadian hydrogen safety program

    International Nuclear Information System (INIS)

    The Canadian hydrogen safety program (CHSP) is a project initiative of the Codes and Standards Working Group of the Canadian transportation fuel cell alliance (CTFCA) that represents industry, academia, government, and regulators. The Program rationale, structure and contents contribute to acceptance of the products, services and systems of the Canadian Hydrogen Industry into the Canadian hydrogen stakeholder community. It facilitates trade through fair insurance policies and rates, effective and efficient regulatory approval procedures and accommodation of the interests of the general public. The Program integrates a consistent quantitative risk assessment methodology with experimental (destructive and non-destructive) failure rates and consequence-of-release data for key hydrogen components and systems into risk assessment of commercial application scenarios. Its current and past six projects include Intelligent Virtual Hydrogen Filling Station (IVHFS), Hydrogen clearance distances, comparative quantitative risk comparison of hydrogen and compressed natural gas (CNG) refuelling options; computational fluid dynamics (CFD) modeling validation, calibration and enhancement; enhancement of frequency and probability analysis, and Consequence analysis of key component failures of hydrogen systems; and fuel cell oxidant outlet hydrogen sensor project. The Program projects are tightly linked with the content of the International Energy Agency (IEA) Task 19 Hydrogen Safety. (author)

  11. Hydrogen energy systems studies

    Energy Technology Data Exchange (ETDEWEB)

    Ogden, J.M.; Steinbugler, M.; Kreutz, T. [Princeton Univ., NJ (United States). Center for Energy and Environmental Studies

    1998-08-01

    In this progress report (covering the period May 1997--May 1998), the authors summarize results from ongoing technical and economic assessments of hydrogen energy systems. Generally, the goal of their research is to illuminate possible pathways leading from present hydrogen markets and technologies toward wide scale use of hydrogen as an energy carrier, highlighting important technologies for RD and D. Over the past year they worked on three projects. From May 1997--November 1997, the authors completed an assessment of hydrogen as a fuel for fuel cell vehicles, as compared to methanol and gasoline. Two other studies were begun in November 1997 and are scheduled for completion in September 1998. The authors are carrying out an assessment of potential supplies and demands for hydrogen energy in the New York City/New Jersey area. The goal of this study is to provide useful data and suggest possible implementation strategies for the New York City/ New Jersey area, as the Hydrogen Program plans demonstrations of hydrogen vehicles and refueling infrastructure. The authors are assessing the implications of CO{sub 2} sequestration for hydrogen energy systems. The goals of this work are (a) to understand the implications of CO{sub 2} sequestration for hydrogen energy system design; (b) to understand the conditions under which CO{sub 2} sequestration might become economically viable; and (c) to understand design issues for future low-CO{sub 2} emitting hydrogen energy systems based on fossil fuels.

  12. Geometrical criteria versus quantum chemical criteria for assessment of intramolecular hydrogen bond (IMHB) interaction: A computational comparison into the effect of chlorine substitution on IMHB of salicylic acid in its lowest energy ground state conformer

    Science.gov (United States)

    Paul, Bijan Kumar; Guchhait, Nikhil

    2013-02-01

    Density functional theory based computational study has been performed to characterize intramolecular hydrogen bonding (IMHB) interaction in a series of salicylic acid derivatives varying in chlorine substitution on the benzene ring. The molecular systems studied are salicylic acid, 5-chlorosalicylic acid, 3,5-dichlorosalicylic acid and 3,5,6-tricholorosalicylic acid. Major emphasis is rendered on the analysis of IMHB interaction by calculation of electron density ρ(r) and Laplacian ∇2ρ(r) at the bond critical point using atoms-in-molecule theory. Topological features, energy densities based on ρ(r) through perturbing the intramolecular H-bond distances suggest that at equilibrium geometry the IMHB interaction develops certain characteristics typical of covalent interaction. The interplay between aromaticity and resonance-assisted hydrogen bonding (RAHB) is discussed using both geometrical and magnetic criteria as the descriptors of aromaticity. The optimized geometry features, molecular electrostatic potential map analysis are also found to produce a consensus view in relation with the formation of RAHB in these systems.

  13. Safety considerations for continuous hydrogen production test apparatus with capacity of 50 N-litter hydrogen per hour

    International Nuclear Information System (INIS)

    Since the thermochemical hydrogen production Iodine-Sulfur process decomposes water into hydrogen and oxygen using toxic chemicals such as sulfuric acid, iodine and hydriodic acid, safety considerations are very important in its research and development. Therefore, before construction of continuous hydrogen production test apparatus with capacity of 50 N-litter hydrogen per hour, comprehensive safety considerations were carried out to examine the design and construction works of the test apparatus, and the experimental plans using the apparatus. Emphasis was given on the safety considerations on prevention of breakage of glasswares and presumable abnormalities, accidents and their countermeasures. This report summarizes the results of the considerations. (author)

  14. Safety considerations for continuous hydrogen production test apparatus with capacity of 50 N-litter hydrogen per hour

    Energy Technology Data Exchange (ETDEWEB)

    Onuki, Kaoru; Akino, Norio; Shimizu, Saburo; Nakajima, Hayato; Higashi, Shunichi; Kubo, Shinji [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment

    2001-03-01

    Since the thermochemical hydrogen production Iodine-Sulfur process decomposes water into hydrogen and oxygen using toxic chemicals such as sulfuric acid, iodine and hydriodic acid, safety considerations are very important in its research and development. Therefore, before construction of continuous hydrogen production test apparatus with capacity of 50 N-litter hydrogen per hour, comprehensive safety considerations were carried out to examine the design and construction works of the test apparatus, and the experimental plans using the apparatus. Emphasis was given on the safety considerations on prevention of breakage of glasswares and presumable abnormalities, accidents and their countermeasures. This report summarizes the results of the considerations. (author)

  15. Hydrogen-ion sputtering of borated graphite

    International Nuclear Information System (INIS)

    The development and choice of material for the first wall and other energy-stressed parts of the discharge chamber are an important aspect of fusion reactor construction. In particular, carbon-graphite materials are proposed for making limiters and protective shields of the first wall and receiving plates of diverter devices. Sputtering under ion bombardment is one of the main mechanisms of material erosion; in addition, in the case of carbon-graphite materials chemical sputtering also occurs as a result of the formation of highly volatile hydrocarbon compounds during the reaction with ions of hydrogen isotopes. Sputtering MPG carbon-graphite materials and USB-15 carbon-fiber-reinforced glass ceramic has been well studied and experimental data have been obtained on the coefficients of physical and chemical sputtering. It has been determined that hydrogen-ion sputtering of USB-15 in the range from room temperature to 1070 K is less than that of MPG-8 graphite a factor of 2-10. Bulk doping of graphite with boron substantially reduces chemical sputtering. Since processes in the surface layers are crucially important in sputtering, the possibility of reducing chemical sputtering by surface boration of carbon-graphite materials has been explored. The objective of this work was to continue the experimental investigation to determine the physical processes of sputtering of surface-borated graphite under hydrogen-ion bombardment in the temperature range corresponding to maximum chemical sputtering. Surface boration of MPG-8 and USB-15 samples was carried out by vapor-phase isothermal deposition mediated by gaseous iodine at 1223 K for 4 h (the sample was placed in a pure boron stock). The mass transfer during the vapor-phase deposition is based on the difference of the chemical potentials of iodine and carbon under isothermal conditions. The samples of the initial and borated carbon-graphite materials irradiated with a poly-energetic beam of hydrogen ions

  16. Allylammonium hydrogen oxalate hemihydrate

    Directory of Open Access Journals (Sweden)

    Błażej Dziuk

    2014-08-01

    Full Text Available In the title hydrated molecular salt, C3H8N+·C2HO4−·0.5H2O, the water O atom lies on a crystallographic twofold axis. The C=C—C—N torsion angle in the cation is 2.8 (3° and the dihedral angle between the CO2 and CO2H planes in the anion is 1.0 (4°. In the crystal, the hydrogen oxalate ions are linked by O—H...O hydrogen bonds, generating [010] chains. The allylammonium cations bond to the chains through N—H...O and N—H...(O,O hydrogen bonds. The water molecule accepts two N—H...O hydrogen bonds and makes two O—H...O hydrogen bonds. Together, the hydrogen bonds generate (100 sheets.

  17. Fiber optic hydrogen sensor

    Science.gov (United States)

    Jung, Chuck C.; Saaski, Elric W.; McCrae, David A.

    1998-09-01

    This paper describes a novel fiber optic-based hydrogen sensor. The sensor consists of a thin-film etalon, constructed on the distal end of a fiber optic. The exterior mirror of the etalon is palladium or a palladium-alloy, which undergoes an optical change upon exposure to hydrogen. Data is presented on fiber optic sensors constructed with palladium and several alloys of palladium. The linearity of the optical response of these sensors to hydrogen is examined. Etalons made with pure palladium are found to be desirable for sensing low concentrations of hydrogen, or for one-time exposure to high concentrations of hydrogen. Etalons made from palladium alloys are found to be more desirable in applications were repeated cycling in high concentrations of hydrogen occurs.

  18. Hydrogen Fuelling Stations

    DEFF Research Database (Denmark)

    Rothuizen, Erasmus Damgaard

    This thesis concerns hydrogen fuelling stations from an overall system perspective. The study investigates thermodynamics and energy consumption of hydrogen fuelling stations for fuelling vehicles for personal transportation. For the study a library concerning the components in a hydrogen fuelling...... station has been developed in Dymola. The models include the fuelling protocol (J2601) for hydrogen vehicles made by Society of Automotive Engineers (SAE) and the thermodynamic property library CoolProp is used for retrieving state point. The components in the hydrogen fuelling library are building up....... A system consisting of one high pressure storage tank is used to investigate the thermodynamics of fuelling a hydrogen vehicle. The results show that the decisive parameter for how the fuelling proceeds is the pressure loss in the vehicle. The single tank fuelling system is compared to a cascade fuelling...

  19. Hydrogen desorption from hydrogen fluoride and remote hydrogen plasma cleaned silicon carbide (0001) surfaces

    Energy Technology Data Exchange (ETDEWEB)

    King, Sean W., E-mail: sean.king@intel.com; Tanaka, Satoru; Davis, Robert F. [Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695 (United States); Nemanich, Robert J. [Department of Physics, North Carolina State University, Raleigh, North Carolina 27695 (United States)

    2015-09-15

    Due to the extreme chemical inertness of silicon carbide (SiC), in-situ thermal desorption is commonly utilized as a means to remove surface contamination prior to initiating critical semiconductor processing steps such as epitaxy, gate dielectric formation, and contact metallization. In-situ thermal desorption and silicon sublimation has also recently become a popular method for epitaxial growth of mono and few layer graphene. Accordingly, numerous thermal desorption experiments of various processed silicon carbide surfaces have been performed, but have ignored the presence of hydrogen, which is ubiquitous throughout semiconductor processing. In this regard, the authors have performed a combined temperature programmed desorption (TPD) and x-ray photoelectron spectroscopy (XPS) investigation of the desorption of molecular hydrogen (H{sub 2}) and various other oxygen, carbon, and fluorine related species from ex-situ aqueous hydrogen fluoride (HF) and in-situ remote hydrogen plasma cleaned 6H-SiC (0001) surfaces. Using XPS, the authors observed that temperatures on the order of 700–1000 °C are needed to fully desorb C-H, C-O and Si-O species from these surfaces. However, using TPD, the authors observed H{sub 2} desorption at both lower temperatures (200–550 °C) as well as higher temperatures (>700 °C). The low temperature H{sub 2} desorption was deconvoluted into multiple desorption states that, based on similarities to H{sub 2} desorption from Si (111), were attributed to silicon mono, di, and trihydride surface species as well as hydrogen trapped by subsurface defects, steps, or dopants. The higher temperature H{sub 2} desorption was similarly attributed to H{sub 2} evolved from surface O-H groups at ∼750 °C as well as the liberation of H{sub 2} during Si-O desorption at temperatures >800 °C. These results indicate that while ex-situ aqueous HF processed 6H-SiC (0001) surfaces annealed at <700 °C remain terminated by some surface C–O and

  20. Experimental results and analysis on hydrogen combustion

    International Nuclear Information System (INIS)

    The Small-Scale Development Apparatus (SSDA) was constructed to provide a preliminary set of experimental data to characterize the effect of temperature on the ability of hydrogen-air-steam-mixtures to undergo detonations and, equally important, to support design of the larger-scale High-Temperature Combustion Facility (HTCF) by providing a test bed for solution of a number of high-temperature design and operational problems. The SSDA, the central element of which is 10-cm inside diameter, 6.1-m long tubular test vessel designed to permit detonation experiments at temperatures up to 700K, was employed to study self-sustained detonations in gaseous mixtures of hydrogen, air, and steam at temperature between 300K and 650K at a fixed pressure of 0.1 MPa. Detonation cell size measurements provide clear evidence that the effect of hydrogen-air gas mixture temperature, in the range 300K to 650K, is to decrease cell size and, hence, to increase the sensitivity of the mixture to undergo detonations. The effect of steam content, at any given temperature, is to increase the cell size and, thereby, to decrease the sensitivity of stoichiometric hydrogen-air mixtures. The one-dimensional ZND model does a very good job at predicting the overall trends in the cell size data over the range of hydrogen-air-steam mixture compositions and temperature studied in the experiments. Experiments were conducted to measure the rate of hydrogen oxidation in the absence of ignition sources at temperatures of 500K and 650K, for hydrogen-air mixtures of 15% and 50%, and for a mixture of equimolar hydrogen-air and 30% steam at 650K. The rate of hydrogen oxidation was found to be significant at 650K. Reduction of hydrogen concentration by chemical reaction from 50 to 44% hydrogen, and from 15 to 11% hydrogen, were observed on a time frame of minutes. The DeSoete rate equation predicts the 50% experiment very well, but greatly underestimates the reaction rate of the lean mixtures

  1. Boron-nitrogen based hydrides and reactive composites for hydrogen storage

    DEFF Research Database (Denmark)

    Jepsen, Lars H.; Ley, Morten B.; Lee, Young-Su;

    2014-01-01

    Hydrogen forms chemical compounds with most other elements and forms a variety of different chemical bonds. This fascinating chemistry of hydrogen has continuously provided new materials and composites with new prospects for rational design and the tailoring of properties. This review highlights...

  2. Hydrogen energy systems studies

    Energy Technology Data Exchange (ETDEWEB)

    Ogden, J.M.; Steinbugler, M.; Dennis, E. [Princeton Univ., NJ (United States)] [and others

    1995-09-01

    For several years, researchers at Princeton University`s Center for Energy and Environmental Studies have carried out technical and economic assessments of hydrogen energy systems. Initially, we focussed on the long term potential of renewable hydrogen. More recently we have explored how a transition to renewable hydrogen might begin. The goal of our current work is to identify promising strategies leading from near term hydrogen markets and technologies toward eventual large scale use of renewable hydrogen as an energy carrier. Our approach has been to assess the entire hydrogen energy system from production through end-use considering technical performance, economics, infrastructure and environmental issues. This work is part of the systems analysis activity of the DOE Hydrogen Program. In this paper we first summarize the results of three tasks which were completed during the past year under NREL Contract No. XR-11265-2: in Task 1, we carried out assessments of near term options for supplying hydrogen transportation fuel from natural gas; in Task 2, we assessed the feasibility of using the existing natural gas system with hydrogen and hydrogen blends; and in Task 3, we carried out a study of PEM fuel cells for residential cogeneration applications, a market which might have less stringent cost requirements than transportation. We then give preliminary results for two other tasks which are ongoing under DOE Contract No. DE-FG04-94AL85803: In Task 1 we are assessing the technical options for low cost small scale production of hydrogen from natural gas, considering (a) steam reforming, (b) partial oxidation and (c) autothermal reforming, and in Task 2 we are assessing potential markets for hydrogen in Southern California.

  3. Hydrogen production by Cyanobacteria

    OpenAIRE

    Chaudhuri Surabhi; De, Debojyoti; Dutta Debajyoti; Bhattacharya Sanjoy K

    2005-01-01

    Abstract The limited fossil fuel prompts the prospecting of various unconventional energy sources to take over the traditional fossil fuel energy source. In this respect the use of hydrogen gas is an attractive alternate source. Attributed by its numerous advantages including those of environmentally clean, efficiency and renew ability, hydrogen gas is considered to be one of the most desired alternate. Cyanobacteria are highly promising microorganism for hydrogen production. In comparison to...

  4. Liquid hydrogen in Japan

    Energy Technology Data Exchange (ETDEWEB)

    Yasumi, S. [Iwatani Corp., Osaka (Japan). Dept. of Overseas Business Development

    2009-07-01

    Japan's Iwatani Corporation has focused its attention on hydrogen as the ultimate energy source in future. Unlike the United States, hydrogen use and delivery in liquid form is extremely limited in the European Union and in Japan. Iwatani Corporation broke through industry stereotypes by creating and building Hydro Edge Co. Ltd., Japan's largest liquid hydrogen plant. It was established in 2006 as a joint venture between Iwatani and Kansai Electric Power Group in Osaka. Hydro Edge is Japan's first combined liquid hydrogen and ASU plant, and is fully operational. Liquid oxygen, liquid nitrogen and liquid argon are separated from air using the cryogenic energy of liquefied natural gas fuel that is used for power generation. Liquid hydrogen is produced efficiently and simultaneously using liquid nitrogen. Approximately 12 times as much hydrogen in liquid form can be transported and supplied as pressurized hydrogen gas. This technology is a significant step forward in the dissemination and expansion of hydrogen in a hydrogen-based economy.

  5. 1H-MAS-NMR Chemical Shifts in Hydrogen-Bonded Complexes of Chlorophenols (Pentachlorophenol, 2,4,6-Trichlorophenol, 2,6-Dichlorophenol, 3,5-Dichlorophenol, and p-Chlorophenol) and Amine, and H/D Isotope Effects on 1H-MAS-NMR Spectra

    OpenAIRE

    Hisashi Honda

    2013-01-01

    Chemical shifts (CS) of the 1H nucleus in N···H···O type hydrogen bonds (H-bond) were observed in some complexes between chlorophenols [pentachlorophenol (PCP), 2,4,6-tricholorophenol (TCP), 2,6-dichlorophenol (26DCP), 3,5-dichlorophenol (35DCP), and p-chlorophenol (pCP)] and nitrogen-base (N-Base) by solid-state high-resolution 1H-NMR with the magic-angle-spinning (MAS) method. Employing N-Bases with a wide range of pKa values (0.65–10.75), 1H-MAS-NMR CS values of bridging H atoms in H-bonds...

  6. Thin films of hydrogenated amorphous carbon (a-C:H) obtained through chemical vapor deposition assisted by plasma; Peliculas delgadas de carbono amorfo hidrogenado (a-C:H) obtenidas mediante deposito quimico de vapores asistido por plasma

    Energy Technology Data Exchange (ETDEWEB)

    Mejia H, J.A.; Camps C, E.E.; Escobar A, L.; Romero H, S.; Chirino O, S. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Muhl S, S. [IIM-UNAM, 04510 Mexico D.F. (Mexico)

    2004-07-01

    Films of hydrogenated amorphous carbon (a-C:H) were deposited using one source of microwave plasma with magnetic field (type ECR), using mixtures of H{sub 2}/CH{sub 4} in relationship of 80/20 and 95/05 as precursory gases, with work pressures of 4X10{sup -4} to 6x10{sup -4} Torr and an incident power of the discharge of microwaves with a constant value of 400 W. It was analyzed the influence among the properties of the films, as the deposit rate, the composition and the bonding types, and the deposit conditions, such as the flow rates of the precursory gases and the polarization voltage of the sample holders. (Author)

  7. Optical determination of the mass density of amorphous and microcrystalline silicon layers with different hydrogen contents

    OpenAIRE

    Remeš, Z.; Vaněček, Milan; Torres, Pedro; Kroll, U.; Mahan, A. H.; Crandall, R. S.

    2008-01-01

    We have measured the density of amorphous and microcrystalline silicon films using an optical method. The mass density decreases with increasing hydrogen content, consistent with a hydrogenated di-vacancy model that fits the data for amorphous silicon. Material produced by hot wire assisted chemical vapour deposition, with low hydrogen content, has a higher density and is structurally different from glow discharge material with hydrogen content around 10 at.%. The lower density microcrystalli...

  8. Evidence of Hydrogen Bonding in Chloroform and Polyacrylates from NMR Measurements

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The presence of hydrogen bonding in chloroform and polyacrylate mixtures was demonstrated by observation of 1H- and 13C-NMR chemical shifts. Comparison of the nuclear magnetic resonance (NMR) chemical shift in polymer solutions with their low molecular mass analogues showed the effect of steric hindrance on hydrogen bonding. This initial investigation is helpful for understanding the intermolecular interaction in relatively weak hydrogen bonding polymer solutions.

  9. HYDROGEN INDUCED CRACKING IN MICROALLOYED STEELS

    Directory of Open Access Journals (Sweden)

    Duberney Hincapie-Ladino

    2015-03-01

    Full Text Available The need for microalloyed steels resistant to harsh environments in oil and gas fields, such as pre-salt which contain considerable amounts of hydrogen sulfide (H2 S and carbon dioxide (CO2 , requires that all sectors involved in petroleum industry know the factors that influence the processes of corrosion and failures by hydrogen in pipelines and components fabricated with microalloyed steels. This text was prepared from a collection of selected publications and research done at the Electrochemical Processes Laboratory of Metallurgical and Materials Engineering Department, Polytechnic School, São Paulo University. This document does not intend to be a complete or exhaustive review of the literature, but rather to address the main scientific and technological factors associated with failures by hydrogen in the presence of wet hydrogen sulfide (H2 S, particularly, when related to the Hydrogen Induced Cracking (HIC phenomenon. This complex phenomenon that involves several successive stages, HIC phenomena were discussed in terms of environmental and metallurgical variables. The HIC starts with the process of corrosion of steel, therefore must be considered the corrosive media (H2 S presence effect. Moreover, it is necessary to know the interactions of compounds present in the electrolyte with the metal surface, and how they affect the hydrogen adsorption and absorption into steel. The following stages are hydrogen diffusion, trapping and metal cracking, directly related to the chemical composition and the microstructure, factors that depend strongly on the manufacture of steel. The purpose of this paper is to provide the scientific information about the failures caused by hydrogen and challenge for the Oil and Gas Pipeline Industry.

  10. Surface analysis, hydrogen adsorption and electrochemical performance of alkali-reduce treated hydrogen storage alloy

    Institute of Scientific and Technical Information of China (English)

    陈卫祥; 徐铸德; 涂江平; 李海洋; 陈石; 袁俊; 鲍世宁

    2002-01-01

    The hydrogen storage alloy powders (MlNi4.0Co0.6Al0.4, Ml=rich-La mischmetal) were treated in a hot 6mol/L KOH+0.02mol/L KBH4 solution, the surface compositions and chemical states of the treated and untreated alloys were analyzed by XPS and EDX, the hydrogen adsorption on the surface of these alloys was evaluated by thermal desorption spectroscopy (TDS), the effects of the surface treatment on the electrochemical performances of the alloy electrodes were investigated. The results show that the hydrogen adsorption is greatly strengthened by the surface modification, and hence leads to marked improvement in the electrocatalytic activity, the treated alloy exhibits higher exchange current density and lower apparent activation energy for the hydrogen electrode reaction than the untreated alloy.

  11. Determination of atomic hydrogen density in non-thermal hydrogen plasmas via emission actinometry

    Energy Technology Data Exchange (ETDEWEB)

    Wang Weiguo [Laboratory of Plasmas Physical Chemistry, PO Box 288, Dalian University of Technology, Dalian 116024 (China); Xu Yong [Laboratory of Plasmas Physical Chemistry, PO Box 288, Dalian University of Technology, Dalian 116024 (China); Geng Zicai [Laboratory of Plasmas Physical Chemistry, PO Box 288, Dalian University of Technology, Dalian 116024 (China); Liu Zhongwei [Laboratory of Plasmas Physical Chemistry, PO Box 288, Dalian University of Technology, Dalian 116024 (China); Zhu Aimin [Laboratory of Plasmas Physical Chemistry, PO Box 288, Dalian University of Technology, Dalian 116024 (China)

    2007-07-21

    Atomic hydrogen plays an important role in the chemical vapour deposition of diamond and other functional materials. This paper reports the experimental determinations of atomic hydrogen density in dielectric barrier discharge hydrogen plasmas via optical emission spectrometry using Ar as an actinometer. At certain discharge conditions (ac 24 kHz, 28 kV of peak-to-peak voltage), the approximate hydrogen dissociation fractions calculated from the emission intensities with respect to electron temperatures obtained with the Langmuir probe, are decreased from 0.099 to 0.01 as the gas pressure increases from 2 to 4 Torr. The relative H atom mole fractions as a function of discharge parameters (spatial position and gas flow rate) have been investigated. It is shown that the discharge characteristics strongly depend on the spatial position but not on the gas flow rate. The influences of the above operating parameters on the emission intensities have been discussed.

  12. Determination of atomic hydrogen density in non-thermal hydrogen plasmas via emission actinometry

    International Nuclear Information System (INIS)

    Atomic hydrogen plays an important role in the chemical vapour deposition of diamond and other functional materials. This paper reports the experimental determinations of atomic hydrogen density in dielectric barrier discharge hydrogen plasmas via optical emission spectrometry using Ar as an actinometer. At certain discharge conditions (ac 24 kHz, 28 kV of peak-to-peak voltage), the approximate hydrogen dissociation fractions calculated from the emission intensities with respect to electron temperatures obtained with the Langmuir probe, are decreased from 0.099 to 0.01 as the gas pressure increases from 2 to 4 Torr. The relative H atom mole fractions as a function of discharge parameters (spatial position and gas flow rate) have been investigated. It is shown that the discharge characteristics strongly depend on the spatial position but not on the gas flow rate. The influences of the above operating parameters on the emission intensities have been discussed

  13. Combined hydrogen production and storage with subsequent carbon crystallization.

    Science.gov (United States)

    Lueking, Angela D; Gutierrez, Humberto R; Fonseca, Dania A; Narayanan, Deepa L; Van Essendelft, Dirk; Jain, Puja; Clifford, Caroline E B

    2006-06-21

    We provide evidence of low-temperature hydrogen evolution and possible hydrogen trapping in an anthracite coal derivative, formed via reactive ball milling with cyclohexene. No molecular hydrogen is added to the process. Raman-active molecular hydrogen vibrations are apparent in samples at atmospheric conditions (300 K, 1 bar) for samples prepared 1 year previously and stored in ambient air. Hydrogen evolves slowly at room temperature and is accelerated upon sample heating, with a first increase in hydrogen evolution occurring at approximately 60 degrees C. Subsequent chemical modification leads to the observation of crystalline carbons, including nanocrystalline diamond surrounded by graphene ribbons, other sp2-sp3 transition regions, purely graphitic regions, and a previously unidentified crystalline carbon form surrounded by amorphous carbon. The combined evidence for hydrogen trapping and carbon crystallization suggests hydrogen-induced crystallization of the amorphous carbon materials, as metastable hydrogenated carbons formed via the high-energy milling process rearrange into more thermodynamically stable carbon forms and molecular hydrogen.

  14. A review on hydrogen production: methods, materials and nanotechnology.

    Science.gov (United States)

    Lang, Yizhao; Arnepalli, Ranga Rao; Tiwari, Ashutosh

    2011-05-01

    In recent years hydrogen production and storage has attracted a lot of attention in both academia and industry due to its variety of applications in energy sector. Hydrogen is recognized as one of the most important components of the next generation clean energy technology. Within the whole cycle of the use of hydrogen energy, hydrogen production is considered as the key element of the upcoming hydrogen economy. Since the first production method invented for hydrogen on a smaller scale by dissolving iron in the acid vitriol in the 15th century, many improvements have been made to make the production viable and more cost effective. It is known that "nano" is playing its role in many technologies from medicine to material science and it has its say even in the production of hydrogen energy with continuous improvements in materials and methodologies. In this review we attempt to list various methods of producing hydrogen from different sources of materials followed by the description of most recent developments in the materials prospective. We explain the role of nanotechnology in making the hydrogen production technology a viable and cost effective process. The chemical reaction cycle, mechanism and configurations of various methods of hydrogen production are elaborated. PMID:21780363

  15. French hydrogen markets in 2008-Overview and future prospects

    International Nuclear Information System (INIS)

    This study analyses the current industrial hydrogen markets in France on both a European and international scale, while endeavouring to assess future prospects by 2030. Hydrogen is produced either on purpose or unintentionally as a co-product. Intentional production of hydrogen, generally from natural gas, is classified as captive or merchant hydrogen. France produces about 920,000 metric tons of hydrogen annually. The producer and consumer industries are, in decreasing order of importance are: oil for refinery and petrochemicals, ammonia, iron and steel (co-production), chemicals, and chlorine (co-production). The intentional production of hydrogen from natural gas amounts to less than that co-produced: 40% compared with 60%. The amount of burned hydrogen is about 25% of the total. Production-related carbon dioxide emissions range between 1% and 2% of the total emissions in France. There is an increasing trend in the industrial hydrogen production, essentially due to the oil industry whereas a decline in production is expected in the ammonia industry. The annual production around 2030 should therefore be greater than 1 million metric tons (MMT) per year. If the iron and steel industry were to use hydrogen in every possible situation, it would double the total quantity of hydrogen produced and consumed in France. (authors)

  16. Mechanical properties of hydrogenated electron-irradiated graphene

    Science.gov (United States)

    Weerasinghe, Asanka; Muniz, Andre R.; Ramasubramaniam, Ashwin; Maroudas, Dimitrios

    2016-09-01

    We report a systematic analysis on the effects of hydrogenation on the mechanical behavior of irradiated single-layer graphene sheets, including irradiation-induced amorphous graphene, based on molecular-dynamics simulations of uniaxial tensile straining tests and using an experimentally validated model of electron-irradiated graphene. We find that hydrogenation has a significant effect on the tensile strength of the irradiated sheets only if it changes the hybridization of the hydrogenated carbon atoms to sp3, causing a reduction in the strength of irradiation-induced amorphous graphene by ˜10 GPa. Hydrogenation also causes a substantial decrease in the failure strain of the defective sheets, regardless of the hybridization of the hydrogenated carbon atoms, and in their fracture toughness, which decreases with increasing hydrogenation for a given irradiation dose. We characterize in detail the fracture mechanisms of the hydrogenated irradiated graphene sheets and elucidate the role of hydrogen and the extent of hydrogenation in the deformation and fracture processes. Our study sets the stage for designing hydrogenation and other chemical functionalization strategies toward tailoring the properties of defect-engineered ductile graphene.

  17. Hydrogen adsorption in metal-decorated silicon carbide nanotubes

    Science.gov (United States)

    Singh, Ram Sevak; Solanki, Ankit

    2016-09-01

    Hydrogen storage for fuel cell is an active area of research and appropriate materials with excellent hydrogen adsorption properties are highly demanded. Nanotubes, having high surface to volume ratio, are promising storage materials for hydrogen. Recently, silicon carbide nanotubes have been predicted as potential materials for future hydrogen storage application, and studies in this area are ongoing. Here, we report a systematic study on hydrogen adsorption properties in metal (Pt, Ni and Al) decorated silicon carbide nanotubes (SiCNTs) using first principles calculations based on density functional theory. The hydrogen adsorption properties are investigated by calculations of adsorption energy, electronic band structure, density of states (DOS) and Mulliken charge population analysis. Our findings show that hydrogen adsorptions on Pt, Ni and Al-decorated SiCNTs undergo spontaneous exothermic reactions with significant modulation of electronic structure of SiCNTs in all cases. Importantly, according to the Mulliken charge population analysis, dipole-dipole interaction causes chemisorptions of hydrogen in Pt, Ni and Al decorated SiCNTs with formation of chemical bonds. The study is a platform for the development of metal decorated SiCNTs for hydrogen adsorption or hydrogen storage application.

  18. Enhancing hydrogen spillover and storage

    Science.gov (United States)

    Yang, Ralph T.; Li, Yingwel; Lachawiec, Jr., Anthony J.

    2011-05-31

    Methods for enhancing hydrogen spillover and storage are disclosed. One embodiment of the method includes doping a hydrogen receptor with metal particles, and exposing the hydrogen receptor to ultrasonification as doping occurs. Another embodiment of the method includes doping a hydrogen receptor with metal particles, and exposing the doped hydrogen receptor to a plasma treatment.

  19. Membrane for hydrogen recovery from streams containing hydrogen sulfide

    Science.gov (United States)

    Agarwal, Pradeep K.

    2007-01-16

    A membrane for hydrogen recovery from streams containing hydrogen sulfide is provided. The membrane comprises a substrate, a hydrogen permeable first membrane layer deposited on the substrate, and a second membrane layer deposited on the first layer. The second layer contains sulfides of transition metals and positioned on the on a feed side of the hydrogen sulfide stream. The present invention also includes a method for the direct decomposition of hydrogen sulfide to hydrogen and sulfur.

  20. EPRI hydrogen research program

    International Nuclear Information System (INIS)

    The need for near-term research on hydrogen behavior as it applies to water reactor safety requires the parallel efforts of a number of organizations. A program has been initiated by EPRI to help answer the most pressing generic questions involving small and large scale combustion, hydrogen mixing, and burn control. Experiments, model development, and code validation work are involved

  1. Hydrogen Storage Tank

    CERN Multimedia

    1983-01-01

    This huge stainless steel reservoir,placed near an end of the East Hall, was part of the safety equipment connected to the 2 Metre liquid hydrogen Bubble Chamber. It could store all the hydrogen in case of an emergency. The picture shows the start of its demolition.

  2. Hydrogen evolution reaction catalyst

    Science.gov (United States)

    Subbaraman, Ram; Stamenkovic, Vojislav; Markovic, Nenad; Tripkovic, Dusan

    2016-02-09

    Systems and methods for a hydrogen evolution reaction catalyst are provided. Electrode material includes a plurality of clusters. The electrode exhibits bifunctionality with respect to the hydrogen evolution reaction. The electrode with clusters exhibits improved performance with respect to the intrinsic material of the electrode absent the clusters.

  3. Thick film hydrogen sensor

    Science.gov (United States)

    Hoffheins, Barbara S.; Lauf, Robert J.

    1995-01-01

    A thick film hydrogen sensor element includes an essentially inert, electrically-insulating substrate having deposited thereon a thick film metallization forming at least two resistors. The metallization is a sintered composition of Pd and a sinterable binder such as glass frit. An essentially inert, electrically insulating, hydrogen impermeable passivation layer covers at least one of the resistors.

  4. Hydrogen bonding in polyanilines

    Energy Technology Data Exchange (ETDEWEB)

    Bahceci, S. (Department of Chemistry, Middle East Technical University, Ankara 06531 (Turkey)); Toppare, L. (Department of Chemistry, Middle East Technical University, Ankara 06531 (Turkey)); Yurtsever, E. (Department of Chemistry, Middle East Technical University, Ankara 06531 (Turkey))

    1994-11-29

    Hydrogen bonding between poly(bisphenol A carbonate) (PC) and polyaniline (PAn) is analyzed using semi-empirical quantum methodology. Fully optimized AM1 molecular orbital calculations are reported for various aniline structures (monomer, dimer and trimer), the monomer of the PC and the hydrogen-bonded model of PAn-PC oligomer. ((orig.))

  5. Dark hydrogen fermentations

    NARCIS (Netherlands)

    Vrije, de G.J.; Claassen, P.A.M.

    2003-01-01

    The production of hydrogen is a ubiquitous, natural phenomenon under anoxic or anaerobic conditions. A wide variety of bacteria, in swamps, sewage, hot springs, the rumen of cattle etc. is able to convert organic matter to hydrogen, CO2 and metabolites like acetic acid, lactate, ethanol and alanine.

  6. Hydrogen Annealing Of Single-Crystal Superalloys

    Science.gov (United States)

    Smialek, James L.; Schaeffer, John C.; Murphy, Wendy

    1995-01-01

    Annealing at temperature equal to or greater than 2,200 degrees F in atmosphere of hydrogen found to increase ability of single-crystal superalloys to resist oxidation when subsequently exposed to oxidizing atmospheres at temperatures almost as high. Supperalloys in question are principal constituents of hot-stage airfoils (blades) in aircraft and ground-based turbine engines; also used in other high-temperature applications like chemical-processing plants, coal-gasification plants, petrochemical refineries, and boilers. Hydrogen anneal provides resistance to oxidation without decreasing fatigue strength and without need for coating or reactive sulfur-gettering constituents. In comparison with coating, hydrogen annealing costs less. Benefits extend to stainless steels, nickel/chromium, and nickel-base alloys, subject to same scale-adhesion and oxidation-resistance considerations, except that scale is chromia instead of alumina.

  7. Proton conducting ceramic membranes for hydrogen separation

    Science.gov (United States)

    Elangovan, S.; Nair, Balakrishnan G.; Small, Troy; Heck, Brian

    2011-09-06

    A multi-phase proton conducting material comprising a proton-conducting ceramic phase and a stabilizing ceramic phase. Under the presence of a partial pressure gradient of hydrogen across the membrane or under the influence of an electrical potential, a membrane fabricated with this material selectively transports hydrogen ions through the proton conducting phase, which results in ultrahigh purity hydrogen permeation through the membrane. The stabilizing ceramic phase may be substantially structurally and chemically identical to at least one product of a reaction between the proton conducting phase and at least one expected gas under operating conditions of a membrane fabricated using the material. In a barium cerate-based proton conducting membrane, one stabilizing phase is ceria.

  8. Study on the hydrogenation coupling of methane

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    At atmospheric pressure and ambient temperature, the hydrogenation coupling of methane was studied by using pulse corona plasma and its synergism with catalyst. The results showed that (ⅰ) under pulse corona plasma, the coupling of methane could be fulfilled by the addition of hydrogen, and with the increase of the amount of hydrogen, the conversion of methane and the yield of C2 hydrocarbon increased, and the deposit of carbon decreased; (ⅱ) the conversion of methane was affected by pulse voltage and repeated frequency; (ⅲ) in the system, the addition of Ni/g-Al2O3 could improve the distribution of C2 hydrocarbon; (ⅳ) the activity of Ni/g-Al2O3 prepared by cold plasma was better than that by chemical methods. The experiment opened up a new technical route of the coupling of methane.

  9. Hydrogen Fuel Quality

    Energy Technology Data Exchange (ETDEWEB)

    Rockward, Tommy [Los Alamos National Laboratory

    2012-07-16

    For the past 6 years, open discussions and/or meetings have been held and are still on-going with OEM, Hydrogen Suppliers, other test facilities from the North America Team and International collaborators regarding experimental results, fuel clean-up cost, modeling, and analytical techniques to help determine levels of constituents for the development of an international standard for hydrogen fuel quality (ISO TC197 WG-12). Significant progress has been made. The process for the fuel standard is entering final stages as a result of the technical accomplishments. The objectives are to: (1) Determine the allowable levels of hydrogen fuel contaminants in support of the development of science-based international standards for hydrogen fuel quality (ISO TC197 WG-12); and (2) Validate the ASTM test method for determining low levels of non-hydrogen constituents.

  10. Hydrogen production methods

    International Nuclear Information System (INIS)

    Old, present and new proceses for producing hydrogen are assessed critically. The emphasis throughout is placed on those processes which could be commercially viable before the turn of the century for large-scale hydrogen manufacture. Electrolysis of water is the only industrial process not dependent on fossil resources for large-scale hydrogen production and is likely to remain so for the next two or three decades. While many new processes, including those utilizing sunlight directly or indirectly, are presently not considered to be commercially viable for large-scale hydrogen production, research and development effort is needed to enhance our understanding of the nature of these processes. Water vapour electrolysis is compared with thermochemical processes: the former has the potential for displacing all other processes for producing hydrogen and oxygen from water

  11. Electrochemical Hydrogen Compressor

    Energy Technology Data Exchange (ETDEWEB)

    Lipp, Ludwig [FuelCell Energy, Inc., Torrington, CT (United States)

    2016-01-21

    Conventional compressors have not been able to meet DOE targets for hydrogen refueling stations. They suffer from high capital cost, poor reliability and pose a risk of fuel contamination from lubricant oils. This project has significantly advanced the development of solid state hydrogen compressor technology for multiple applications. The project has achieved all of its major objectives. It has demonstrated capability of Electrochemical Hydrogen Compression (EHC) technology to potentially meet the DOE targets for small compressors for refueling sites. It has quantified EHC cell performance and durability, including single stage hydrogen compression from near-atmospheric pressure to 12,800 psi and operation of EHC for more than 22,000 hours. Capital cost of EHC was reduced by 60%, enabling a path to meeting the DOE cost targets for hydrogen compression, storage and delivery ($2.00-2.15/gge by 2020).

  12. Implementing a hydrogen economy

    Directory of Open Access Journals (Sweden)

    James A Ritter

    2003-09-01

    In recent years, months, weeks, and even days, it has become increasingly clear that hydrogen as an energy carrier is ‘in’ and carbonaceous fuels are ‘out’1. The hydrogen economy is coming, with the impetus to transform our fossil energy-based society, which inevitably will cease to exist, into a renewable energy-based one2. However, this transformation will not occur overnight. It may take several decades to realize a hydrogen economy. In the meantime, research and development is necessary to ensure that the implementation of the hydrogen economy is completely seamless, with essentially no disruption of the day-to-day activities of the global economy. The world has taken on a monumental, but not insurmountable, task of transforming from carbonaceous to renewable fuels, with clean burning, carbon dioxide-free hydrogen as the logical choice.

  13. sup 1 H NMR studies of a biosynthetic lacto-ganglio hybrid glycosphingolipid: Confirmation of structure, interpretation of anomalous' chemical shifts, and evidence for interresidue amide-amide hydrogen bonding

    Energy Technology Data Exchange (ETDEWEB)

    Levery, S.B.; Harris, D.D.; Hakomori, Senitiroh (Univ. of Washington, Seattle (United States)); Holmes, E.H. (Pacific Northwest Research Foundation, Seattle, WA (United States))

    1992-02-04

    Glycosphinogolipids bearing GlcNAc{beta}1 {yields} 3 and GalNAc{beta}1 {yields} 4 linked to {beta}-Gal of lactosylceramide first isolated from a murine myelogenous leukemia cell line have since been found as normal components of mullet roe and English sole liver. In order to clarify the biosynthetic pathways responsible for its occurrence both as a product of normal tissues and as a possible mammalian cancer-associated antigen, the lacto-ganglio hybrid core structure LcGg{sub 4}Cer was synthesized from Lc{sub 3}Cer using a GalNAc{beta}1 {yields} 4 transferase preparation from English sole liver. A preliminary characterization of the enzyme, which may be identical to the GalNAc T-1 responsible for synthesis of GM{sub 2} ganglioside, is presented. The enzymatically synthesized product was analyzed by 1- and 2-D {sup 1}H NMR spectroscopy, confirming its primary structure as GalNAc{beta}1 {yields} 4-(GlcNAc{beta}1 {yields} 3)Gal{beta}1 {yields} 4Glc{beta}1 {yields} 1Cer. An approximate three-dimensional structure for LcGg{sub 4}Cer is proposed, consistent with all data obtained, which should be useful in discussing the results of {sup 1}H NMR analysis of compounds containing this core tetrasaccharide. The structure is characterized by an unusual arrangement of terminal N-acetylhexosamine residues, resulting in a {pi}-H hydrogen-bonding interaction between their acetamido groups.

  14. Photolytic Decomposition Of Hydrogen Sulfide In The Gas Mixtures And Formation Of Molecular Hydrogen

    International Nuclear Information System (INIS)

    Full text : The chemical conversions of organic fuels during the refining processes complex gas mixtures containing hydrogen sulfide generate as a by-product. In accordance with the environmental safety requirements these gas mixtures have to be purified from hydrogen sulfide before use or environmental discharge. As it is known because of combustion gases containing hydrogen-sulfide oxides of sulfide emit into the atmosphere and they combine with water vapors in the air and this process consequently results in pH change of H2SO3 precipitations and acid rains. The processes of purification of gas mixtures being the product of oil refining processes and mainly containing hydrocarbons from hydrogen sulfide by a photochemical method and molecular hydrogen generation have been under this investigation.The model gas mixture under investigation has been prepared at a vacuum plant in the laboratory. During the researches the partial pressure of H2S capable of completely absorbing the given wave-length of the radiation has been first specified. It has been established that temperature and irradiation time have their influence on the progress rate of the processes.At this wave-length hydrocarbons undergo no photochemical conversions. This is manifested with the absence of excitation levels causing dissociation due to radiation absorption at the wave-length used in hydrocarbon gases . The fact that these levels belong to hydrogen sulfide contained in gas mixtures has been experimentally proved.The role of hot hydrogen atoms and the mechanism of the processes under progress within the process of molecular hydrogen generation due to the photolytic decomposition of hydrogen sulfide have been discussed.

  15. Hydrogen production processes; Procedes de production d'hydrogene

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2003-07-01

    The goals of this first Gedepeon workshop on hydrogen production processes are: to stimulate the information exchange about research programs and research advances in the domain of hydrogen production processes, to indicate the domains of interest of these processes and the potentialities linked with the coupling of a nuclear reactor, to establish the actions of common interest for the CEA, the CNRS, and eventually EDF, that can be funded in the framework of the Gedepeon research group. This document gathers the slides of the 17 presentations given at this workshop and dealing with: the H{sub 2} question and the international research programs (Lucchese P.); the CEA's research program (Lucchese P., Anzieu P.); processes based on the iodine/sulfur cycle: efficiency of a facility - flow-sheets, efficiencies, hard points (Borgard J.M.), R and D about the I/S cycle: Bunsen reaction (Colette S.), R and D about the I/S cycle: the HI/I{sub 2}/H{sub 2}O system (Doizi D.), demonstration loop/chemical engineering (Duhamet J.), materials and corrosion (Terlain A.); other processes under study: the Westinghouse cycle (Eysseric C.), other processes under study at the CEA (UT3, plasma,...) (Lemort F.), database about thermochemical cycles (Abanades S.), Zn/ZnO cycle (Broust F.), H{sub 2} production by cracking, high temperature reforming with carbon trapping (Flamant G.), membrane technology (De Lamare J.); high-temperature electrolysis: SOFC used as electrolyzers (Grastien R.); generic aspects linked with hydrogen production: technical-economical evaluation of processes (Werkoff F.), thermodynamic tools (Neveu P.), the reactor-process coupling (Aujollet P.). (J.S.)

  16. Low Cost Hydrogen Production Platform

    Energy Technology Data Exchange (ETDEWEB)

    Timothy M. Aaron, Jerome T. Jankowiak

    2009-10-16

    A technology and design evaluation was carried out for the development of a turnkey hydrogen production system in the range of 2.4 - 12 kg/h of hydrogen. The design is based on existing SMR technology and existing chemical processes and technologies to meet the design objectives. Consequently, the system design consists of a steam methane reformer, PSA system for hydrogen purification, natural gas compression, steam generation and all components and heat exchangers required for the production of hydrogen. The focus of the program is on packaging, system integration and an overall step change in the cost of capital required for the production of hydrogen at small scale. To assist in this effort, subcontractors were brought in to evaluate the design concepts and to assist in meeting the overall goals of the program. Praxair supplied the overall system and process design and the subcontractors were used to evaluate the components and system from a manufacturing and overall design optimization viewpoint. Design for manufacturing and assembly (DFMA) techniques, computer models and laboratory/full-scale testing of components were utilized to optimize the design during all phases of the design development. Early in the program evaluation, a review of existing Praxair hydrogen facilities showed that over 50% of the installed cost of a SMR based hydrogen plant is associated with the high temperature components (reformer, shift, steam generation, and various high temperature heat exchange). The main effort of the initial phase of the program was to develop an integrated high temperature component for these related functions. Initially, six independent concepts were developed and the processes were modeled to determine overall feasibility. The six concepts were eventually narrowed down to the highest potential concept. A US patent was awarded in February 2009 for the Praxair integrated high temperature component design. A risk analysis of the high temperature component was

  17. Protein Chemical Shift Prediction

    CERN Document Server

    Larsen, Anders S

    2014-01-01

    The protein chemical shifts holds a large amount of information about the 3-dimensional structure of the protein. A number of chemical shift predictors based on the relationship between structures resolved with X-ray crystallography and the corresponding experimental chemical shifts have been developed. These empirical predictors are very accurate on X-ray structures but tends to be insensitive to small structural changes. To overcome this limitation it has been suggested to make chemical shift predictors based on quantum mechanical(QM) calculations. In this thesis the development of the QM derived chemical shift predictor Procs14 is presented. Procs14 is based on 2.35 million density functional theory(DFT) calculations on tripeptides and contains corrections for hydrogen bonding, ring current and the effect of the previous and following residue. Procs14 is capable at performing predictions for the 13CA, 13CB, 13CO, 15NH, 1HN and 1HA backbone atoms. In order to benchmark Procs14, a number of QM NMR calculatio...

  18. Hydrogenated liquids and hydrogen production by non-thermal plasmas

    Energy Technology Data Exchange (ETDEWEB)

    Arabi, K.; Aubry, O.; Khacef, A.; Cormier, J.M. [Orleans Univ., Orleans Cedex (France). Centre national de la recherche scientifique, Polytech d' Orleans, Group for Research and Studies on Mediators of Inflamation

    2010-07-01

    In recent years, hydrogen (H{sub 2}) has been considered as a fuel for electricity generation and transportation purposes. H{sub 2} is a renewable energy source that does not contribute to the greenhouse effect. This paper reported on a comparative study of syngas production from alcohol, with particular reference to the plasma steam-reforming of ethanol, methanol, ammonia and vegetable oil. The H{sub 2} yields and energetic cost in function of hydrogen sources were presented. The non thermal plasma used in this study was a laboratory scale experimental device static discharge. An arc formed between two electrodes made of graphite. The efficiency of the process was determined through chemical diagnostics. Gas chromatography and Fourier transform infrared (FTIR) techniques were used to determine concentrations of H{sub 2}, carbon monoxide, carbon dioxide and carbon as functions of flow and inlet liquid mixture concentration parameters. This paper also presented the values of H{sub 2}/CO ratio and the composition of synthesis gas according to various operating conditions. 18 refs., 2 tabs., 8 figs.

  19. Superconductivity for hydrogen economy

    International Nuclear Information System (INIS)

    The emerging hydrogen economy is expected to deal with a large amount of liquid hydrogen produced from the renewable energy resources. The main advantage of liquid hydrogen in comparison with other forms of its storage and transportation is in allowing wide use of superconductivity, which would optimise energy efficiency of the economy. The basic element of the infrastructure for hydrogen economy is a network of superconducting pipelines carrying simultaneously liquid hydrogen and loss-free electricity. The most likely material for such infrastructure is MgB2, the only superconductor efficiently working at boiling temperature of liquid hydrogen and not showing strong critical current reduction on grain boundaries. The cheap techniques for the preparation of MgB2 are hot isostatic pressing, resistive sintering and paint coating. These and other advanced techniques are able to provide MgB2 with suitable for the infrastructure structural and superconducting properties. The preparation of a large-area superconducting joint between two pieces of MgB2 as a technique enabling this infrastructure is reported. A potential of synergy between liquid hydrogen and superconductivity is revealed in a range of possible new energy applications.

  20. Photoelectrochemical hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Rocheleau, R.; Misra, A.; Miller, E. [Univ. of Hawaii, Honolulu, HI (United States)

    1998-08-01

    A significant component of the US DOE Hydrogen Program is the development of a practical technology for the direct production of hydrogen using a renewable source of energy. High efficiency photoelectrochemical systems to produce hydrogen directly from water using sunlight as the energy source represent one of the technologies identified by DOE to meet this mission. Reactor modeling and experiments conducted at UH provide strong evidence that direct solar-to-hydrogen conversion efficiency greater than 10% can be expected using photoelectrodes fabricated from low-cost, multijunction (MJ) amorphous silicon solar cells. Solar-to-hydrogen conversion efficiencies as high as 7.8% have been achieved using a 10.3% efficient MJ amorphous silicon solar cell. Higher efficiency can be expected with the use of higher efficiency solar cells, further improvement of the thin film oxidation and reduction catalysts, and optimization of the solar cell for hydrogen production rather than electricity production. Hydrogen and oxygen catalysts developed under this project are very stable, exhibiting no measurable degradation in KOH after over 13,000 hours of operation. Additional research is needed to fully optimize the transparent, conducting coatings which will be needed for large area integrated arrays. To date, the best protection has been afforded by wide bandgap amorphous silicon carbide films.

  1. Chemical use

    Data.gov (United States)

    US Fish and Wildlife Service, Department of the Interior — This is a summary of research and activities related to chemical use on Neal Smith National Wildlife Refuge between 1992 and 2009. The chemicals used on the Refuge...

  2. Chemical Reactors.

    Science.gov (United States)

    Kenney, C. N.

    1980-01-01

    Describes a course, including content, reading list, and presentation on chemical reactors at Cambridge University, England. A brief comparison of chemical engineering education between the United States and England is also given. (JN)

  3. A liquid organic carrier of hydrogen as a fuel for automobiles

    International Nuclear Information System (INIS)

    A system of storing energy in a hydrogen containing fuel for the motor car is discussed. The recyclable liquid chemical carrier is: (Methylcyclohexane (liquid)) dehydrogenation (Toluene (liquid)) + (hydrogen (gas)). The reverse reaction, the hydrogenation of toluene, occurs in a regional plant connected to a source of hydrogen (electrolysis of water) with a significant by-product being heat at 200 0C for district heating. The system is able to store hydrogen in liquid form under ambient temperature and pressure even in a small motor car. The concentration of hydrogen is 6.1 % by weight. The release of gaseous hydrogen from the liquid methylcyclohexane needs a chemical catalytic reactor having a temperature of 300 0C and a pressure of some bars. This reaction has been well studied. The thermal energy for the dehydrogenation is taken from the exhaust gases at 780 0C. A layout of the most important processes of the system is given. (Auth.)

  4. Hydrogen storage in graphite nanofibres : new developments

    Energy Technology Data Exchange (ETDEWEB)

    Shutz, W. [Vodafone Pilotentwicklung GmbH, Munich (Germany); Maneck, E. [Bundesanstalt fur Materialforschung, Berlin (Germany)

    2002-07-01

    Carbon materials show high potential as candidates for hydrogen storage for automotive applications, but the price of hydrogen-driven vehicles is too high and customer acceptance is low. In this study, carbon nanofibers were synthesized through the reaction of carbon containing gases over a suitable catalyst. Essentially, carbon nanofibres were created by chemical catalytic vapour deposition of carbon containing gases using a horizontal quartz tube reactor at 500 to 1000 degrees C. The size and shape of the product was found to be dependent on the catalyst used and by the reaction temperature and time. The presentation illustrates gravimetric and volumetric storage capacity measurements, pressure dependent X-ray diffraction and temperature programmed desorption spectroscopy measurements. It was shown that the intercalated hydrogen in carbon nanofibers can be released during heating. Future studies will focus on examining the effects of the interaction between carbon nanofibers and hydrogen with focus on the potential of these materials for technical use in hydrogen storage systems. 7 refs., 2 figs.

  5. Nanomaterials for Hydrogen Storage Applications: A Review

    Directory of Open Access Journals (Sweden)

    Michael U. Niemann

    2008-01-01

    Full Text Available Nanomaterials have attracted great interest in recent years because of the unusual mechanical, electrical, electronic, optical, magnetic and surface properties. The high surface/volume ratio of these materials has significant implications with respect to energy storage. Both the high surface area and the opportunity for nanomaterial consolidation are key attributes of this new class of materials for hydrogen storage devices. Nanostructured systems including carbon nanotubes, nano-magnesium based hydrides, complex hydride/carbon nanocomposites, boron nitride nanotubes, TiS2/MoS2 nanotubes, alanates, polymer nanocomposites, and metal organic frameworks are considered to be potential candidates for storing large quantities of hydrogen. Recent investigations have shown that nanoscale materials may offer advantages if certain physical and chemical effects related to the nanoscale can be used efficiently. The present review focuses the application of nanostructured materials for storing atomic or molecular hydrogen. The synergistic effects of nanocrystalinity and nanocatalyst doping on the metal or complex hydrides for improving the thermodynamics and hydrogen reaction kinetics are discussed. In addition, various carbonaceous nanomaterials and novel sorbent systems (e.g. carbon nanotubes, fullerenes, nanofibers, polyaniline nanospheres and metal organic frameworks etc. and their hydrogen storage characteristics are outlined.

  6. Biological hydrogen formation by thermophilic bacteria

    OpenAIRE

    Bielen, A.A.M.

    2014-01-01

      Hydrogen gas (H2) is an important chemical commodity. It is used in many industrial processes and is applicable as a fuel. However, present production processes are predominantly based on non-renewable resources. In a biological H2 (bioH2) production process, known as dark-fermentation, fermentative microorganisms are able to generate H2 from renewable resources like carbohydrate-rich plant material or industrial waste streams. Because of their favourable biomass degrading capabilities...

  7. Hydrogen sulfide prodrugs—a review

    Directory of Open Access Journals (Sweden)

    Yueqin Zheng

    2015-09-01

    Full Text Available Hydrogen sulfide (H2S is recognized as one of three gasotransmitters together with nitric oxide (NO and carbon monoxide (CO. As a signaling molecule, H2S plays an important role in physiology and shows great potential in pharmaceutical applications. Along this line, there is a need for the development of H2S prodrugs for various reasons. In this review, we summarize different H2S prodrugs, their chemical properties, and some of their potential therapeutic applications.

  8. Hydrogen sulfide prodrugs—a review

    Science.gov (United States)

    Zheng, Yueqin; Ji, Xingyue; Ji, Kaili; Wang, Binghe

    2015-01-01

    Hydrogen sulfide (H2S) is recognized as one of three gasotransmitters together with nitric oxide (NO) and carbon monoxide (CO). As a signaling molecule, H2S plays an important role in physiology and shows great potential in pharmaceutical applications. Along this line, there is a need for the development of H2S prodrugs for various reasons. In this review, we summarize different H2S prodrugs, their chemical properties, and some of their potential therapeutic applications. PMID:26579468

  9. Photobiological hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Seibert, M.; Lien, S.; Weaver, P.F.

    1979-01-01

    Hydrogen production by phototrophic organisms, which has been known since the 1930's, occurs at the expense of light energy and electron-donating substrates. Three classes of organisms, namely, photosynthetic bacteria, cyanobacteria, and algae carry out this function. The primary hydrogen-producing enzyme systems, hydrogenase and nitrogenase, will be discussed along with the manner in which they couple to light-driven electron transport. In addition, the feasibility of using in vivo and in vitro photobiological hydrogen producing systems in future solar energy conversion applications will be examined.

  10. Photobiological hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Seibert, M; Lien, S; Weaver, P F

    1979-01-01

    Hydrogen production by phototrophic organisms, which has been known since the 1930's, occurs at the expense of light energy and electron-donating substrates. Three classes of organisms, namely, photosynthetic bacteria, cyanobacteria, and algae carry out this function. The primary hydrogen-producing enzyme systems, hydrogenase and nitrogenase, will be discussed along with the manner in which they couple to light-driven electron transport. In addition, the feasibility of using in vivo and in vitro photobiological hydrogen producing systems in future solar energy conversion applications will be examined.

  11. National hydrogen energy roadmap

    Energy Technology Data Exchange (ETDEWEB)

    None, None

    2002-11-01

    This report was unveiled by Energy Secretary Spencer Abraham in November 2002 and provides a blueprint for the coordinated, long-term, public and private efforts required for hydrogen energy development. Based on the results of the government-industry National Hydrogen Energy Roadmap Workshop, held in Washington, DC on April 2-3, 2002, it displays the development of a roadmap for America's clean energy future and outlines the key barriers and needs to achieve the hydrogen vision goals defined in

  12. A hydrogen utopia?

    Energy Technology Data Exchange (ETDEWEB)

    Cherry, Robert S. [National Academy of Engineering, Washington, DC (United States)

    2004-02-01

    The use of hydrogen as a fuel for transportation and stationary applications is receiving much favorable attention as a technical and policy issue. However, the widespread introduction of this technology is likely also to have negative consequences that are not being actively discussed in broad public forums. Such possibilities include, among others, delayed development of other energy alternatives, hazards of catalyst or hydride metals, disruptive employment shifts, land usage conflicts, and increased vehicle usage. Even though hydrogen is likely to be beneficial in its overall societal and environmental effects, hydrogen technology advocates must understand the range of problematic issues and prepare to address them. (Author)

  13. A Hydrogen Utopia?

    Energy Technology Data Exchange (ETDEWEB)

    Cherry, Robert Stephen; Reynolds, Bruce Allen

    2004-01-01

    The use of hydrogen as a fuel for transportation and stationary applications is receiving much favorable attention as a technical and policy issue. However, the widespread introduction of this technology is likely also to have negative consequences that are not being actively discussed in broad public forums. Such possibilities include, among others, delayed development of other energy alternatives, hazards of catalyst or hydride metals, disruptive employment shifts, land usage conflicts, and increased vehicle usage. Even though hydrogen is likely to be beneficial in its overall societal and environmental effects, hydrogen technology advocates must understand the range of problematic issues and prepare to address them.

  14. Inside the Hydrogen Atom

    CERN Document Server

    Nowakowski, M; Fierro, D Bedoya; Manjarres, A D Bermudez

    2016-01-01

    We apply the non-linear Euler-Heisenberg theory to calculate the electric field inside the hydrogen atom. We will demonstrate that the electric field calculated in the Euler-Heisenberg theory can be much smaller than the corresponding field emerging from the Maxwellian theory. In the hydrogen atom this happens only at very small distances. This effect reduces the large electric field inside the hydrogen atom calculated from the electromagnetic form-factors via the Maxwell equations. The energy content of the field is below the pair production threshold.

  15. Biological hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Benemann, J.R. [Univ. of California, Berkeley, CA (United States)

    1995-11-01

    Biological hydrogen production can be accomplished by either thermochemical (gasification) conversion of woody biomass and agricultural residues or by microbiological processes that yield hydrogen gas from organic wastes or water. Biomass gasification is a well established technology; however, the synthesis gas produced, a mixture of CO and H{sub 2}, requires a shift reaction to convert the CO to H{sub 2}. Microbiological processes can carry out this reaction more efficiently than conventional catalysts, and may be more appropriate for the relatively small-scale of biomass gasification processes. Development of a microbial shift reaction may be a near-term practical application of microbial hydrogen production.

  16. Hydrogen production from water: Recent advances in photosynthesis research

    Energy Technology Data Exchange (ETDEWEB)

    Greenbaum, E.; Lee, J.W. [Oak Ridge National Lab., TN (United States). Chemical Technology Div.

    1997-12-31

    The great potential of hydrogen production by microalgal water splitting is predicated on quantitative measurement of the algae`s hydrogen-producing capability, which is based on the following: (1) the photosynthetic unit size of hydrogen production; (2) the turnover time of photosynthetic hydrogen production; (3) thermodynamic efficiencies of conversion of light energy into the Gibbs free energy of molecular hydrogen; (4) photosynthetic hydrogen production from sea water using marine algae; (5) the potential for research advances using modern methods of molecular biology and genetic engineering to maximize hydrogen production. ORNL has shown that sustained simultaneous photoevolution of molecular hydrogen and oxygen can be performed with mutants of the green alga Chlamydomonas reinhardtii that lack a detectable level of the Photosystem I light reaction. This result is surprising in view of the standard two-light reaction model of photosynthesis and has interesting scientific and technological implications. This ORNL discovery also has potentially important implications for maximum thermodynamic conversion efficiency of light energy into chemical energy by green plant photosynthesis. Hydrogen production performed by a single light reaction, as opposed to two, implies a doubling of the theoretically maximum thermodynamic conversion efficiency from {approx}10% to {approx}20%.

  17. Chemical sensor

    Science.gov (United States)

    Rauh, R. David (Inventor)

    1990-01-01

    A sensor for detecting a chemical substance includes an insertion element having a structure which enables insertion of the chemical substance with a resulting change in the bulk electrical characteristics of the insertion element under conditions sufficient to permit effective insertion; the change in the bulk electrical characteristics of the insertion element is detected as an indication of the presence of the chemical substance.

  18. Biomimetic hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Krassen, Henning

    2009-05-15

    Hydrogenases catalyze the reduction of protons to molecular hydrogen with outstanding efficiency. An electrode surface which is covered with active hydrogenase molecules becomes a promising alternative to platinum for electrochemical hydrogen production. To immobilize the hydrogenase on the electrode, the gold surface was modified by heterobifunctional molecules. A thiol headgroup on one side allowed the binding to the gold surface and the formation of a self-assembled monolayer. The other side of the molecules provided a surface with a high affinity for the hydrogenase CrHydA1 from Chlamydomonas reinhardtii. With methylviologen as a soluble energy carrier, electrons were transferred from carboxy-terminated electrodes to CrHydA1 and conducted to the active site (H-cluster), where they reduce protons to molecular hydrogen. A combined approach of surface-enhanced infrared absorption spectroscopy, gas chromatography, and surface plasmon resonance allowed quantifying the hydrogen production on a molecular level. Hydrogen was produced with a rate of 85 mol H{sub 2} min{sup -1} mol{sup -1}. On a 1'- benzyl-4,4'-bipyridinum (BBP)-terminated surface, the electrons were mediated by the monolayer and no soluble electron carrier was necessary to achieve a comparable hydrogen production rate (approximately 50% of the former system). The hydrogen evolution potential was determined to be -335 mV for the BBP-bound hydrogenase and -290 mV for the hydrogenase which was immobilized on a carboxy-terminated mercaptopropionic acid SAM. Therefore, both systems significantly reduce the hydrogen production overpotential and allow electrochemical hydrogen production at an energy level which is close to the commercially applied platinum electrodes (hydrogen evolution potential of -270 mV). In order to couple hydrogen production and photosynthesis, photosystem I (PS1) from Synechocystis PCC 6803 and membrane-bound hydrogenase (MBH) from Ralstonia eutropha were bound to each other

  19. In situ NMR study of hydrogenation/dehydrogenation of ZrCr{sub 2} and physisorbed hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, Jamil, E-mail: mjasomba@gmail.com [Graduate School of Engineering, Tohoku University (Japan); Maekawa, Hideki; Takamura, Hitoshi; Oikawa, Itaru; Ando, Mariko; Takahashi, Kuniaki [Graduate School of Engineering, Tohoku University (Japan)

    2012-11-05

    Highlights: Black-Right-Pointing-Pointer In situ NMR study of hydrogenation of C14-ZrCr{sub 2}. Black-Right-Pointing-Pointer Observation of physisorbed hydrogen peak in NMR spectra. Black-Right-Pointing-Pointer Change of chemical shift of physisorbed H{sub 2} ({delta}{sub phy}) with degree of hydrogenation. Black-Right-Pointing-Pointer Linearity between {delta}{sub phy} and degree of hydrogenation. Black-Right-Pointing-Pointer Linearity between degree of hydrogenation and density of states, N{sub d}(E{sub F}). - Abstract: In situ proton nuclear magnetic resonance (NMR) was employed to study the hydrogenation and dehydrogenation kinetics of ZrCr{sub 2}. The powder samples prepared by arc melting followed by homogenizing heat treatment and grinding were put inside a boron nitride (BN) crucible, which was placed inside a quartz tube attached to a high pressure assembly specially designed for in situ NMR measurements. The samples were activated at 573 K under vacuum inside the high temperature probe and then exposed to the required hydrogen gas pressure at room temperature for hydrogenation. Gradual hydrogenation of the samples was recorded through in situ NMR. Before activation of the sample, the exposure to high pressure showed two peaks with NMR shifts of 8.5 and -3.3 ppm, which were assigned to hydrogen gas and physisorbed hydrogen, respectively. After activation, the sample showed absorption manifested through the appearance of a broad peak with an NMR shift of -141 ppm. The NMR shift of absorption peak increased to higher magnetic fields as the hydrogen absorption proceeded. It was also accompanied by a change in NMR shift of physisorbed hydrogen peak in the same direction. Both the shifts, i.e., of absorbed hydrogen as well as of physisorbed hydrogen were linearly related with the degree of hydrogenation. This change in NMR shift of physisorbed hydrogen was explained on the basis of increase in density of d-electronic states at Fermi level with an increase in

  20. Advanced Catalytic Hydrogenation Retrofit Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Reinaldo M. Machado

    2002-08-15

    Industrial hydrogenation is often performed using a slurry catalyst in large stirred-tank reactors. These systems are inherently problematic in a number of areas, including industrial hygiene, process safety, environmental contamination, waste production, process operability and productivity. This program proposed the development of a practical replacement for the slurry catalysts using a novel fixed-bed monolith catalyst reactor, which could be retrofitted onto an existing stirred-tank reactor and would mitigate many of the minitations and problems associated with slurry catalysts. The full retrofit monolith system, consisting of a recirculation pump, gas/liquid ejector and monolith catalyst, is described as a monolith loop reactor or MLR. The MLR technology can reduce waste and increase raw material efficiency, which reduces the overall energy required to produce specialty and fine chemicals.

  1. Hydrogenation of 9-ethylcarbazole as a prototype of a liquid hydrogen carrier

    Energy Technology Data Exchange (ETDEWEB)

    Eblagon, Katarzyna Morawa; Tsang, Shik Chi [Wolfson Catalysis Centre, Inorganic Chemistry Laboratory, University of Oxford, Oxford OX1 3QR (United Kingdom); Rentsch, Daniel [Laboratory for Functional Polymers, Swiss Federal Laboratories for Materials Testing and Research, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland); Friedrichs, Oliver; Remhof, Arndt; Zuettel, Andreas [Hydrogen and Energy Empa - Swiss Federal Laboratories for Materials Testing and Research, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland); Ramirez-Cuesta, A.J. [ISIS facility, Rutherford Appleton Laboratory, Chilton, Didcot OX11 0QX (United Kingdom)

    2010-10-15

    Liquid organic hydrides, e.g. 9-ethylcarbazole, are potentially interesting hydrogen storage materials because of their reversible hydrogen sorption properties. In the present work, hydrogenation reaction of 9-ethylcarbazole in the molten form was investigated over a wide variety of noble metal and nickel supported catalysts. The catalytic activity of 8.2 x 10{sup -6} mol-ethylcarbazole/g of metal/s and selectivity of 98% towards a fully hydrogen loaded product were recorded over 5 wt% ruthenium on alumina which was prepared by mild chemical reduction of ruthenium salt. Using this catalyst the theoretical capacity of hydrogen uptake (5.7 wt%) was obtained and the rate of the reaction and activation energy were estimated. Due to its potential high hydrogen storage capacity, this system could be a promising on-board storage candidate for mobile applications. The structures of reaction products and intermediates were identified using 2D NMR techniques. These structures were also predicted to be thermodynamically stable using density functional theory (DFT), matching well with the experimental observations. (author)

  2. Statistical Parameters for Hydrogen Bonding Networks: One Component Case

    Institute of Scientific and Technical Information of China (English)

    王海军; 洪晓钟; 赵敏; 巴信武

    2001-01-01

    Based on the analysis of network structures formed by hydrogen bonds as the sol-gel phase transition takesplace in a single component hydrogen bonding system, the theory of reversible gelation is applied to calculatesome statistical parameters that determine many physical and chemical properties of the networks. Then, thentunerical simulation of the number of active chains and dangling chains, the number of effective cross-linkages,the number of active and dangling mers and the modulus as a function of conversion are undertaken.

  3. Heterogeneous hydrogenation catalysts

    International Nuclear Information System (INIS)

    The main types of heterogeneous catalysts used for hydrogenation, the methods for their preparation, and the structure and chemistry of their surfaces are considered, as well as the catalytic activity and the mechanism of action in the hydrogenation of unsaturated and aromatic compounds, of CO, and of carbonyl compounds and in the hydrorefining of fuels. Chief attention is paid to supported Ni catalysts, to the methods for their preparation and physicochemical studies, and to the development of novel catalytic systems through modification. A novel type of catalyst for hydrogenation, viz. metal carbides, is described. Some aspects of the mechanochemical treatment of hydrogenation catalysts, including in situ methods, are discussed. Sulfide catalysts for hydrotreating are also discussed in detail. The bibliography includes 340 references.

  4. Hydrogen Recovery System Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Rocket test operations at NASA Stennis Space Center (SSC) result in substantial quantities of hydrogen gas that is flared from the facility and helium gas that is...

  5. Fiber optic hydrogen sensor

    Energy Technology Data Exchange (ETDEWEB)

    Butler, M.A.; Sanchez, R.; Dulleck, G.R.

    1996-05-01

    This report covers the development of fiber optic hydrogen and temperature sensors for monitoring dissolved hydrogen gas in transformer oil. The concentration of hydrogen gas is a measure of the corona and spark discharge within the transformer and reflects the state of health of the transformer. Key features of the instrument include use of palladium alloys to enhance hydrogen sensitivity, a microprocessor controlled instrument with RS-232, liquid crystal readout, and 4-20 ma. current loop interfaces. Calibration data for both sensors can be down loaded to the instrument through the RS-232 interface. This project was supported by the Technology Transfer Initiative in collaboration with J. W. Harley, Inc. through the mechanism of a cooperative research and development agreement (CRADA).

  6. Interstitial hydrogen storage system

    Energy Technology Data Exchange (ETDEWEB)

    Gell, H.A.

    1980-09-30

    A metal hydride fuel system is described that incorporates a plurality of storage elements that may be individually replaced to provide a hydrogen fuel system for combustion engines having a capability of partial refueling is presented.

  7. Hydrogen on the rise

    Science.gov (United States)

    2016-08-01

    Using hydrogen as an energy carrier has long been discussed as a route to a greener future, and although headway has been less significant than many hoped, recent developments point to tangible progress.

  8. Hydrogen Recovery System Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Liquid hydrogen is used extensively by NASA to support cryogenic rocket testing. In addition, there are many commercial applications in which delivery and use of...

  9. Hydrogen Bonding in Hydrogenated Amorphous Germanium

    Institute of Scientific and Technical Information of China (English)

    M.S.Abo-Ghazala; S. Al Hazmy

    2004-01-01

    Thin films of hydrogenated amorphous germanium (a-Ge:H) were prepared by radio frequency glow discharge deposition at various substrate temperatures. The hydrogen distribution and bonding structure in a-Ge:H were discussed based on infrared absorption data. The correlation between infrared absorption spectra and hydrogen effusion measurements was used to determine the proportionality constant for each vibration mode of the Ge-H bonds. The results reveal that the bending mode appearing at 835 cm?1 is associated with the Ge-H2 (dihydride) groups on the internal surfaces of voids. While 1880 cm?1 is assigned to vibrations of Ge-H (monohydride) groups in the bulk, the 2000 cm?1 stretching mode is attributed to Ge-H and Ge-H2 bonds located on the surfaces of voids. For films associated with bending modes in the infrared spectra, the proportionality constant values of the stretching modes near 1880 and 2000 cm?1 are found to be lower than those of films which had no corresponding bending modes.

  10. Chemical Leukoderma.

    Science.gov (United States)

    Bonamonte, Domenico; Vestita, Michelangelo; Romita, Paolo; Filoni, Angela; Foti, Caterina; Angelini, Gianni

    2016-01-01

    Chemical leukoderma, often clinically mimicking idiopathic vitiligo and other congenital and acquired hypopigmentation, is an acquired form of cutaneous pigment loss caused by exposure to a variety of chemicals that act through selective melanocytotoxicity. Most of these chemicals are phenols and aromatic or aliphatic catechols derivatives. These chemicals, however, are harmful for melanocytes in individuals with an individual susceptibility. Nowadays, chemical leukoderma is fairly common, caused by common domestic products. The presence of numerous acquired confetti- or pea-sized macules is clinically characteristic of chemical leukoderma, albeit not diagnostic. Other relevant diagnostic elements are a history of repeated exposure to a known or suspected depigmenting agent at the sites of onset and a macules distribution corresponding to sites of chemical exposure. Spontaneous repigmentation has been reported when the causative agent is avoided; the repigmentation process is perifollicular and gradual, taking place for a variable period of weeks to months. PMID:27172302

  11. The hydrogen issue.

    Science.gov (United States)

    Armaroli, Nicola; Balzani, Vincenzo

    2011-01-17

    Hydrogen is often proposed as the fuel of the future, but the transformation from the present fossil fuel economy to a hydrogen economy will need the solution of numerous complex scientific and technological issues, which will require several decades to be accomplished. Hydrogen is not an alternative fuel, but an energy carrier that has to be produced by using energy, starting from hydrogen-rich compounds. Production from gasoline or natural gas does not offer any advantage over the direct use of such fuels. Production from coal by gasification techniques with capture and sequestration of CO₂ could be an interim solution. Water splitting by artificial photosynthesis, photobiological methods based on algae, and high temperatures obtained by nuclear or concentrated solar power plants are promising approaches, but still far from practical applications. In the next decades, the development of the hydrogen economy will most likely rely on water electrolysis by using enormous amounts of electric power, which in its turn has to be generated. Producing electricity by burning fossil fuels, of course, cannot be a rational solution. Hydroelectric power can give but a very modest contribution. Therefore, it will be necessary to generate large amounts of electric power by nuclear energy of by renewable energies. A hydrogen economy based on nuclear electricity would imply the construction of thousands of fission reactors, thereby magnifying all the problems related to the use of nuclear energy (e.g., safe disposal of radioactive waste, nuclear proliferation, plant decommissioning, uranium shortage). In principle, wind, photovoltaic, and concentrated solar power have the potential to produce enormous amounts of electric power, but, except for wind, such technologies are too underdeveloped and expensive to tackle such a big task in a short period of time. A full development of a hydrogen economy needs also improvement in hydrogen storage, transportation and distribution

  12. The hydrogen issue.

    Science.gov (United States)

    Armaroli, Nicola; Balzani, Vincenzo

    2011-01-17

    Hydrogen is often proposed as the fuel of the future, but the transformation from the present fossil fuel economy to a hydrogen economy will need the solution of numerous complex scientific and technological issues, which will require several decades to be accomplished. Hydrogen is not an alternative fuel, but an energy carrier that has to be produced by using energy, starting from hydrogen-rich compounds. Production from gasoline or natural gas does not offer any advantage over the direct use of such fuels. Production from coal by gasification techniques with capture and sequestration of CO₂ could be an interim solution. Water splitting by artificial photosynthesis, photobiological methods based on algae, and high temperatures obtained by nuclear or concentrated solar power plants are promising approaches, but still far from practical applications. In the next decades, the development of the hydrogen economy will most likely rely on water electrolysis by using enormous amounts of electric power, which in its turn has to be generated. Producing electricity by burning fossil fuels, of course, cannot be a rational solution. Hydroelectric power can give but a very modest contribution. Therefore, it will be necessary to generate large amounts of electric power by nuclear energy of by renewable energies. A hydrogen economy based on nuclear electricity would imply the construction of thousands of fission reactors, thereby magnifying all the problems related to the use of nuclear energy (e.g., safe disposal of radioactive waste, nuclear proliferation, plant decommissioning, uranium shortage). In principle, wind, photovoltaic, and concentrated solar power have the potential to produce enormous amounts of electric power, but, except for wind, such technologies are too underdeveloped and expensive to tackle such a big task in a short period of time. A full development of a hydrogen economy needs also improvement in hydrogen storage, transportation and distribution

  13. Cryogenic hydrogen release research.

    Energy Technology Data Exchange (ETDEWEB)

    LaFleur, Angela Christine [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2015-12-01

    The objective of this project was to devolop a plan for modifying the Turbulent Combustion Laboratory (TCL) with the necessary infrastructure to produce a cold (near liquid temperature) hydrogen jet. The necessary infrastructure has been specified and laboratory modifications are currently underway. Once complete, experiments from this platform will be used to develop and validate models that inform codes and standards which specify protection criteria for unintended releases from liquid hydrogen storage, transport, and delivery infrastructure.

  14. Pionic hydrogen and deuterium

    Energy Technology Data Exchange (ETDEWEB)

    Gotta, Detlev, E-mail: d.gotta@fz-juelich.de [Forschungszentrum Juelich GmbH and JHCP (Germany); Amaro, F. D. [Coimbra University, Department of Physics (Portugal); Anagnostopoulos, D. F. [University of Ioannina, Department of Materials Science and Engineering (Greece); Buehler, P. [Austrian Academy of Sciences, SMI (Austria); Gorke, H. [Forschungszentrum Juelich GmbH and JHCP (Germany); Covita, D. S. [Coimbra University, Department of Physics (Portugal); Fuhrmann, H.; Gruber, A. [Austrian Academy of Sciences, SMI (Austria); Hennebach, M. [Forschungszentrum Juelich GmbH and JHCP (Germany); Hirtl, A.; Ishiwatari, T. [Austrian Academy of Sciences, SMI (Austria); Indelicato, P.; Bigot, E.-O. Le [LKB, UPMC-Paris 6, ENS, CNRS, Case 74 (France); Marton, J. [Austrian Academy of Sciences, SMI (Austria); Nekipelov, M. [Forschungszentrum Juelich GmbH and JHCP (Germany); Santos, J. M. F. dos [Coimbra University, Department of Physics (Portugal); Schlesser, S. [LKB, UPMC-Paris 6, ENS, CNRS, Case 74 (France); Schmid, Ph. [Austrian Academy of Sciences, SMI (Austria); Simons, L. M. [Paul Scherrer Institut (PSI) (Switzerland); Strauch, Th. [Forschungszentrum Juelich GmbH and JHCP (Germany); and others

    2012-05-15

    The ground-state level shifts and broadenings of the hydrogen isotopes caused by the strong interaction have been redetermined by using a high-resolution crystal spectrometer. An additional measurement of muonic hydrogen reveals properties of the de-excitation cascade of such electrically neutral exotic atoms, in particular Coulomb de-excitation, the understanding of which is essential for the analysis of the hadronic-atom data.

  15. Removal of Hydrogen Sulphide from Water

    Directory of Open Access Journals (Sweden)

    S. Edwards

    2011-01-01

    Full Text Available Problem statement: The concentration of H2S in groundwater is a significant problem in various areas across Canada. Hydrogen sulphide dissolves in ground water imparting undesirable taste and irritating rotten egg smell which makes it unpalatable. Ingestion of sulphides through drinking water can result in stomach discomfort, nausea and vomiting. Humans exposed to high concentrations of H2S for prolonged periods show symptoms of gastro-intestinal upset, anorexia, nausea, somnolence, amnesia, loss of consciousness, delirium, hallucinations, difficulty in swallowing, low blood pressure, slowing of heart rate, double vision and epileptiform convulsions. Hydrogen sulphide in blood is rapidly oxidized by molecular oxygen and thus reduces the oxidation power of haemoglobin. Unoxidized hydrogen sulphide can act upon the central nervous system and cause either paralysis or respiratory failure. It is therefore, necessary to have a very low concentration of H2S in the water. Approach: An automatic system for the addition of KMnO4 and removal of hydrogen sulphide from ground water was developed and tested. The system consisted of a freshwater tank, a pump, a chemical storage tank, a solenoid valve, a photocell and electronic circuit, a drainage tank, a filter and a set of valves. It was possible to use a photocell to detect the presence of excess KMnO4 in the system and to control the addition of KMnO4 into the system. Results: The system accomplished complete removal of hydrogen sulphide in the range of 1-30 ppm. The present system utilizes on/off control for the addition of the chemical. The amount of KMnO4 needed as a percentage of the amount used was in the range of 5-28%. Conclusion: The photocell and circuit could be used to add an amount of chemical that is constantly proportional to the amount of hydrogen sulphide in the water. The control of a positive displacement chemical feed pump would be an ideal application for this system. The speed of the

  16. A continuum damage analysis of hydrogen attack in a 2.25Cr–1Mo pressure vessel

    NARCIS (Netherlands)

    Burg, M.W.D. van der; Giessen, E. van der; Tvergaard, V.

    1998-01-01

    A micromechanically based continuum damage model is presented to analyze the stress, temperature and hydrogen pressure dependent material degradation process termed hydrogen attack, inside a pressure vessel. Hydrogen attack (HA) is the damage process of grain boundary facets due to a chemical reacti

  17. Determining the Energetics of the Hydrogen Bond through FTIR: A Hands-On Physical Chemistry Lab Experiment

    Science.gov (United States)

    Guerin, Abby C.; Riley, Kristi; Rupnik, Kresimir; Kuroda, Daniel G.

    2016-01-01

    Hydrogen bonds are very important chemical structures that are responsible for many unique and important properties of solvents, such as the solvation power of water. These distinctive features are directly related to the stabilization energy conferred by hydrogen bonds to the solvent. Thus, the characterization of hydrogen bond energetics has…

  18. Utilization of chemical looping strategy in coal gasification processes

    Institute of Scientific and Technical Information of China (English)

    Liangshih Fan; Fanxing Li; Shwetha Ramkumar

    2008-01-01

    Three chemical looping gasification processes, i. e. Syngas Chemical Looping (SCL) process, Coal Direct Chemical Looping (CDCL) process, and Calcium Looping process (CLP), are being developed at the Ohio State University (OSU). These processes utilize simple reaction schemes to convert carbonaceous fuels into products such as hydrogen, electricity, and synthetic fuels through the transformation of a highly reactive, highly recyclable chemical intermediate. In this paper, these novel chemical looping gasification processes are described and their advantages and potential challenges for commercialization are discussed.

  19. Examining hydrogen transitions.

    Energy Technology Data Exchange (ETDEWEB)

    Plotkin, S. E.; Energy Systems

    2007-03-01

    This report describes the results of an effort to identify key analytic issues associated with modeling a transition to hydrogen as a fuel for light duty vehicles, and using insights gained from this effort to suggest ways to improve ongoing modeling efforts. The study reported on here examined multiple hydrogen scenarios reported in the literature, identified modeling issues associated with those scenario analyses, and examined three DOE-sponsored hydrogen transition models in the context of those modeling issues. The three hydrogen transition models are HyTrans (contractor: Oak Ridge National Laboratory), MARKAL/DOE* (Brookhaven National Laboratory), and NEMS-H2 (OnLocation, Inc). The goals of these models are (1) to help DOE improve its R&D effort by identifying key technology and other roadblocks to a transition and testing its technical program goals to determine whether they are likely to lead to the market success of hydrogen technologies, (2) to evaluate alternative policies to promote a transition, and (3) to estimate the costs and benefits of alternative pathways to hydrogen development.

  20. Hydrogen isotope technology

    International Nuclear Information System (INIS)

    Hydrogen pumping speeds on panels of molecular sieve types 5A and Na-Y were compared for a variety of sieve (and chevron) temperatures between 10 and 30 K. Although pumping speeds declined with time, probably because of the slow diffusion of hydrogen from the surface of the sieve crystals into the internal regions, the different sieve materials and operating conditions could be compared using time-averaged pump speeds. The (average) pumping speeds declined with increasing temperature. Under some conditions, the Na-Y sieve performed much better than the 5A sieve. Studies of the effect of small concentrations (approx. 4%) of hydrogen on helium pumping indicate that compound cryopumps in fusion reactors will not have to provide complete screening of hydrogen from helium panels. The concentrations of hydrogen did not lower effective helium pumping speeds or shorten the helium operating period between instabilities. Studies of tritium recovery from blankets of liquid lithium focused on design and construction of a flowing-lithium test system and on ultimate removal of tritium from yttrium sorbents. At 5050C, tritium release from yttrium behaves as a diffusion-controlled process, but the release rates are very low. Apparently, higher temperatures will be required for effective sorbent regeneration. An innovative technique for separating hydrogen isotopes by using bipolar electrolysis with permeable electrodes was analyzed to determine its potential usefulness in multistage separation